Home Cart 0 Sign in  

[ CAS No. 888731-75-7 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
HazMat Fee +

There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 888731-75-7
Chemical Structure| 888731-75-7
Structure of 888731-75-7 * Storage: {[proInfo.prStorage]}
Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Quality Control of [ 888731-75-7 ]

Related Doc. of [ 888731-75-7 ]

Alternatived Products of [ 888731-75-7 ]

Product Details of [ 888731-75-7 ]

CAS No. :888731-75-7 MDL No. :MFCD18393154
Formula : C7H4Cl2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 191.01 Pubchem ID :-
Synonyms :

Safety of [ 888731-75-7 ]

Signal Word:Danger Class:6.1,8
Precautionary Statements:P260-P264-P280-P301+P330+P331+P310-P303+P361+P353+P310+P363-P304+P340+P310-P305+P351+P338+P310-P405-P501 UN#:2928
Hazard Statements:H301-H311-H314-H331 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 888731-75-7 ]

* 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.

  • Downstream synthetic route of [ 888731-75-7 ]

[ 888731-75-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 34113-69-4 ]
  • [ 888731-75-7 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride; In N,N-dimethyl-formamide; toluene; Step 1 Production of 4-chloro-3-hydroxybenzoyl chloride 4-Chloro-3-hydroxybenzoic acid (510 mg) was suspended in toluene (6 mL), and thionyl chloride (0.28 mL) and N,N-dimethylformamide (1 drop) were added. After stirring with heating at 70 C. for 2 hrs, and the mixture was concentrated and azeotroped with toluene to give the title compound.
With thionyl chloride; In tetrahydrofuran; dichloromethane; at 50℃; for 2h; A mixture of <strong>[34113-69-4]4-chloro-3-hydroxybenzoic acid</strong> (5 g, 29 mmol) and thionyl chloride (31 ml, 0.43 mol) in CH2Cl2/tetrahydrofuran (1:1; 50 ml) is stirred for 2 h at 50 C. The reaction mixture is evaporated in vacuo. After addition of CH2Cl2 (50 ml), the mixture is cooled to 5 C. and treated by dropwise addition of cyclopropylamine (8.1 ml, 115 mmol) during 1 h. The cooling bath is removed and the reaction stirred for 14 h at RT. After dilution with CH2Cl2, the organic phase is washed with a saturated NaHCO3-solution and part of the solvent is removed in vacuo. The crystals thus formed are filtered off and dried to afford 4-chloro-N-cyclopropyl-3-hydroxy-benzamide as white crystals. MS: 212.2 [M+H]+; tR (HPLC, Nucleosil C18; 5-100% CH3CN+0.1% TFA/H2O+0.1% TFA for 8 min, flow 1.5 ml/min): 4.12 min.
With thionyl chloride; In N,N-dimethyl-formamide; toluene; at 70℃; for 2h; Step 1 Production of 4-chloro-3-hydroxybenzoyl chloride 4-Chloro-3-hydroxybenzoic acid (510 mg) was suspended in toluene (6 mL), and thionyl chloride (0.28 mL) and N,N-dimethylformamide (1 drop) were added. After stirring with heating at 70 C. for 2 hrs, and the mixture was concentrated and azeotroped with toluene to give the title compound.
With thionyl chloride;N,N-dimethyl-formamide; In toluene; at 70℃; for 2h; Step 1 Production of 4-chloro-3-hydroxybenzoyl chloride 4-Chloro-3-hydroxybenzoic acid (510 mg) was suspended in toluene (6 mL), and thionyl chloride (0.28 mL) and N,N-dimethylformamide (1 drop) were added. After stirring with heating at 70 C. for 2 hrs, and the mixture was concentrated and azeotroped with toluene to give the title compound.

Same Skeleton Products
Historical Records