Purity | Size | Price | VIP Price | USA Stock *0-1 Day | Global Stock *5-7 Days | Quantity | |||||
{[ item.p_purity ]} | {[ item.pr_size ]} |
{[ getRatePrice(item.pr_usd, 1,1) ]} {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate) ]} |
{[ getRatePrice(item.pr_usd, 1,1) ]} | Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate) ]} {[ getRatePrice(item.pr_usd,1,item.mem_rate) ]} | {[ item.pr_usastock ]} | Inquiry - | {[ item.pr_chinastock ]} | Inquiry - |
* Storage: {[proInfo.prStorage]}
CAS No. : | 548-61-8 | MDL No. : | MFCD00137820 |
Formula : | C19H19N3 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | ADUMIBSPEHFSLA-UHFFFAOYSA-N |
M.W : | 289.37 | Pubchem ID : | 68356 |
Synonyms : |
Leucopararosaniline
|
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P501-P261-P273-P272-P280-P302+P352-P362+P364-P333+P313 | UN#: | N/A |
Hazard Statements: | H317-H412 | Packing Group: | N/A |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With acetic acid; zinc |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With ethanol; ammonia at 150℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
79% | With hydrogen In tetrahydrofuran for 12h; | |
With hydrogenchloride; zinc | ||
With ammonium sulfide |
With ethanol; sodium hydrogensulfite; zinc in der Siedehitze; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With hydrogenchloride; mercury dichloride at 150℃; | ||
With pyridine; copper chloride; air at 100℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With hydrogenchloride Diazotization.Behandeln der Diazoniumsalzloesung mit CuCl, NaCl und konz. Salzsaeure; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With hydrogenchloride; zinc |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With ethanol |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With aniline hydrochloride at 100℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With aniline hydrochloride at 170℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With zinc(II) chloride at 170℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With sulfuric acid; 2,4,6-Trinitrophenol at 140 - 150℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
70% | With acetic acid In ethanol at 50℃; for 10h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
71% | With acetic acid In ethanol at 50℃; for 18h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
31% | In dichloromethane Ambient temperature; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With methanol; sodium tetrahydroborate; sodium hydroxide; at 20℃; for 1h; | EX 11 was prepared by reduction of pararosaniline hydrochloride. Specifically, 115.18 g of pararosaniline hydrochloride, 200 mL of methanol, 11.1 mL of SN Sodium hydroxide, and 1 .86 g Sodium Borohydride were stirred at room temperature for about 1 hour. Then the pH was adjusted to 7-9 and the product precipitated out. Filter to collect product. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
75% | With pyridine at 80℃; for 10h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
35% | With acetic acid In ethanol at 70℃; for 24h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
45% | With pyridine; triphenyl phosphite at 100℃; for 12h; | |
43% | With pyridine; triphenyl phosphite at 90℃; for 12h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
31% | With 1,8-diazabicyclo[5.4.0]undec-7-ene In various solvent(s) at 100℃; | |
With 1,8-diazabicyclo[5.4.0]undec-7-ene In various solvent(s) at 100℃; for 5h; Yield given; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
68% | With pyridine; triphenyl phosphite In various solvent(s) at 90℃; for 12h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
15% | With pyridine; triphenyl phosphite at 90℃; for 12h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With zinc(II) chloride at 120 - 140℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With aniline hydrochloride | ||
With aniline hydrochloride |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With aniline hydrochloride at 100 - 110℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
77% | In dichloromethane at 20℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
62% | at 220℃; for 8h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
90% | In tetrahydrofuran; acetonitrile at 20℃; for 240h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: 35 percent / glacial AcOH / ethanol / 24 h / 70 °C 2: 30 percent / 50percent HNO3 / dioxane; H2O / 20 h / 95 - 100 °C |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: 70 percent / glacial AcOH / ethanol / 10 h / 50 °C 2: 23 percent / conc. HNO3, NaNO2 / dioxane; H2O / 10 h / Heating |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: 75 percent / pyridine / 10 h / 80 °C 2: 60 percent / CrO3, glacial AcOH / H2O / 5 h / 40 - 80 °C |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: 110 - 115 °C / auf dem Wasserbade 2: benzene; alcohol; sodium amalgam |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: ZnCl2 2: zinc; hydrochloric acid |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With 4-methyl-morpholine In water; N,N-dimethyl-formamide | R.75 Synthesis of tris[4-(β-benzyloxycarbonylaminomethyl-L-alanyl) aminophenyl]methane hydrochloride Reference Example 75 Synthesis of tris[4-(β-benzyloxycarbonylaminomethyl-L-alanyl) aminophenyl]methane hydrochloride Tris(4-aminophenyl)methane (145 mg), β-benzyloxycarbonylaminomethyl-N-t-butoxycarbonyl-L-alanine (618 mg) and N-methylmorpholine (172 mg) were dissolved in N,N-dimethylformamide (3 ml), after which an N,N-dimethylformamide solution containing O-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (0.825 M, 2 ml) was added while cooling on ice, the temperature was raised to room temperature, and the mixture was stirred for 14 hours. The reaction mixture was poured into water (20 mL) and shaken. This was then centrifuged, and the supernatant was removed. After adding saturated sodium bicarbonate water (20 mL) to the residue and stirring, the mixture was centrifuged and the supernatant was removed. The procedure of centrifugation and removal of the supernatant was then carried out once with saturated sodium bicarbonate water (20 mL) and twice with water (20 mL). The residue was dried under reduced pressure to obtain tris[4-(β-benzyloxycarbonylaminomethyl-N-t-butoxycarbonyl-L-alanyl)aminophenyl]methane. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
89% | With triethylamine In dichloromethane |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
85% | With triethylamine In dichloromethane |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
80% | With triethylamine In dichloromethane |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
93% | With triethylamine In dichloromethane |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
90% | With triethylamine In dichloromethane |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
95% | With triethylamine In dichloromethane |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
92% | With triethylamine In dichloromethane |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
77% | With triethylamine In dichloromethane |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
79% | With triethylamine In dichloromethane |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
80% | With triethylamine In dichloromethane |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
78% | With triethylamine In dichloromethane |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
89% | In ethanol at 20℃; for 168h; Inert atmosphere; | 4,4',4''-[methanetriyltris(benzene-4,1-diyl)tris(azanylylidene)]tris(methanylylidene)}tribenzoic acid (4a) A solution of 4-formylbenzoic acid (189mg, 1.25 mmol) in absolute ethanol (15 mL) was addedinto a stirred solution of 4,4’,4’’-triaminotriphenylmethane 5 (110 mg, 0.38 mmol) inabsolute ethanol (40 mL), in a pre-dried 100 mL singleneckround-bottomed flask equipped with a magneticstirrer. The resulting mixture was stirred for seven daysat room temperature, under an atmosphere of drynitrogen. The reaction mixture was then filtered under suction on a sintered funnel to give a greyishpink solid which was washed with absolute ethanol (60 mL). Purification of the solid was performedby column chromatography on silica gel (9 : 1 : 0.15, CHCl3 : MeOH : Et3N) to afford product 4a as agrey solid (232 mg, 89%) |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
63% | In ethanol at 20℃; for 240h; Inert atmosphere; | 4',4''',4'''''-[Methanetriyltris(benzene-4,1-diyl)tris(azanylylidene)]tris(methanylylidene)}tris(1,1'-biphenyl)-4'-carboxylicacid (4b) A solution of 4-(4-formylphenyl)benzoic acid 8 (203 mg, 0.89mmol) in absolute ethanol (15 mL) wasadded into a stirred solution of 4,4’,4’’-triaminotriphenylmethane 5 (78.6 mg, 0.27mmol) in absolute ethanol (35 mL), in a dry100 mL single-neck round-bottomed flask.The resulting mixture was stirred for tendays at room temperature, under an atmosphere of dry nitrogen. The reaction mixture was then filteredunder suction on a sintered funnel to give an off-white solid which was washed successively withEtOH, CHCl3, acetonitrile, THF and finally with ether. Residual solvent traces were removed underhigh vacuum to afford product 4b as an off-white solid (157 mg, 63%). |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With copper(ll) sulfate pentahydrate In tetrahydrofuran for 3h; Autoclave; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With copper(ll) sulfate pentahydrate In tetrahydrofuran at 120℃; for 3h; Autoclave; |
[ 2479-47-2 ]
4,4'-(Propane-2,2-diyl)dianiline
Similarity: 0.96
[ 6962-10-3 ]
4-(2-Phenylpropan-2-yl)aniline
Similarity: 0.96
[ 60532-63-0 ]
4,4',4'',4'''-Methanetetrayltetraaniline
Similarity: 0.96
[ 1416354-38-5 ]
4-(2-Phenylpropan-2-yl)aniline hydrochloride
Similarity: 0.92
[ 2479-47-2 ]
4,4'-(Propane-2,2-diyl)dianiline
Similarity: 0.96
[ 6962-10-3 ]
4-(2-Phenylpropan-2-yl)aniline
Similarity: 0.96
[ 60532-63-0 ]
4,4',4'',4'''-Methanetetrayltetraaniline
Similarity: 0.96
[ 1416354-38-5 ]
4-(2-Phenylpropan-2-yl)aniline hydrochloride
Similarity: 0.92