Home Cart 0 Sign in  
X

[ CAS No. 5306-96-7 ] {[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+
3d Animation Molecule Structure of 5306-96-7
Chemical Structure| 5306-96-7
Chemical Structure| 5306-96-7
Structure of 5306-96-7 * Storage: {[proInfo.prStorage]}
Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Quality Control of [ 5306-96-7 ]

Related Doc. of [ 5306-96-7 ]

Alternatived Products of [ 5306-96-7 ]

Product Details of [ 5306-96-7 ]

CAS No. :5306-96-7 MDL No. :MFCD00058687
Formula : C8H12N2 Boiling Point : -
Linear Structure Formula :- InChI Key :GZVVXXLYQIFVCA-UHFFFAOYSA-N
M.W : 136.19 Pubchem ID :145785
Synonyms :

Safety of [ 5306-96-7 ]

Signal Word:Danger Class:8
Precautionary Statements:P280-P305+P351+P338-P310 UN#:3259
Hazard Statements:H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 5306-96-7 ]

* 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 [ 5306-96-7 ]

[ 5306-96-7 ] Synthesis Path-Downstream   1~20

  • 2
  • 3,3,4,4-tetramethyl-cyclopentane-1,2-dione [ No CAS ]
  • [ 5306-96-7 ]
  • 2-(4-dimethylamino-phenylimino)-3,3,4,4-tetramethyl-cyclopentanone [ No CAS ]
YieldReaction ConditionsOperation in experiment
at 100℃;
  • 3
  • [ 5306-96-7 ]
  • 2,3-dimethyl-[1,4]benzoquinone-bis-chlorimin [ No CAS ]
YieldReaction ConditionsOperation in experiment
With acetic acid; calcium chloride at 0℃;
  • 4
  • [ 618-06-4 ]
  • [ 87-59-2 ]
  • [ 5306-96-7 ]
YieldReaction ConditionsOperation in experiment
Spalten der gebildeten Azoverbindung mit Zinn und Salzsaeure;
  • 5
  • [ 5306-96-7 ]
  • [ 556-61-6 ]
  • [ 16349-70-5 ]
  • 6
  • [ 5306-96-7 ]
  • [ 74960-06-8 ]
YieldReaction ConditionsOperation in experiment
41% With N-sulfinylmethanesulfonamide
  • 7
  • [ 75-44-5 ]
  • [ 5306-96-7 ]
  • 2,3-dimethylphenylene-1,4-diisocyanate [ No CAS ]
YieldReaction ConditionsOperation in experiment
43% In various solvent(s) for 0.5h; Heating;
  • 8
  • [ 7647-01-0 ]
  • [ 53877-42-2 ]
  • [ 5306-96-7 ]
  • [ 87-59-2 ]
YieldReaction ConditionsOperation in experiment
das Dihydrochlorid reagiert;
  • 10
  • [ 87-59-2 ]
  • [ 5306-96-7 ]
YieldReaction ConditionsOperation in experiment
With water Erhitzen der erhaltenen Azo-Verbindung mit wss.Mineralsaeure und Zink;
  • 12
  • [ 15568-85-1 ]
  • [ 5306-96-7 ]
  • [ 503864-10-6 ]
YieldReaction ConditionsOperation in experiment
With trimethyl orthoformate for 1h; Heating;
  • 13
  • [ 134-98-5 ]
  • [ 5306-96-7 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: HNO3+H2SO4 / <0 / man verseift die Acetverbindungen mit verd.Salzsaeure 2: zinc; water
  • 14
  • [ 5306-96-7 ]
  • 4,5,<i>N</i>,<i>N</i>'-tetramethyl-benzo[1,2-<i>d</i>;4,3-<i>d</i>']bisthiazole-2,7-diamine [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 2: Br2 / CHCl3
YieldReaction ConditionsOperation in experiment
Nonlimiting examples of suitable aromatic diamines, aminophenols, polyhydric phenols and derivatives thereof, respectively, are the following compounds: ... 4-amino-N-ethyl-N-(β-sulfoethyl)aniline, 3-methyl-4-amino-N-ethyl-N-(β-sulfoethyl)aniline, N-(4-aminophenyl)morpholine, N-(4-aminophenyl)piperidine, 2,3-dimethyl-p-phenylenediamine, 2-isopropyl-p-phenylenediamine, N,N-bis-(2-hydroxyethyl)-p-phenylenediamine sulfate, o-aminophenol, ...
Nonlimiting examples of suitable aromatic diamines, aminophenols, polyhydric phenols and derivatives thereof, respectively, are the following compounds: ... 2-(4-nitrobenzyl)-p-phenylenediamine, 2-(4-methylphenyl)-p-phenylenediamine, 2-(2,5-diaminophenyl)-5-methylbenzoic acid, 2-methoxy-p-phenylenediamine, 2,3-dimethyl-p-phenylenediamine, 2,5-dimethyl-p-phenylenediamine, 2-methyl-5-methoxy-p-phenylenediamine, 2,6-methyl-5-methoxy-p-phenylenediamine, ...
The process of claim 3 wherein said compound of formula (II) is selected from the group consisting of ... methoxy-para-phenylenediamine, chloro-para-phenylenediamine, 2,6-dimethyl-para-phenylenediamine, 2,5-dimethyl-para-phenylenediamine, 2,3-dimethyl-para-phenylenediamine, 2,6-diethyl-para-phenylenediamine, 2-methyl-5-methoxy-para-phenylenediamine, 2,6-dimethyl-5-methoxy-para-phenylenediamine, ...
The process of claim 1 wherein said paraphenylenediamine of formula I is selected from the group consisting of ... N-furfuryl paraphenylenediamine, 3-methoxy-N'-methyl paraphenylenediamine, 2-chloro paraphenylenediamine, N-methyl paraphenylenediamine, 2,3-dimethylparaphenylenediamine, 5-chloro-N'-methyl paraphenylenediamine, 5-methyl-N',N'-dimethyl paraphenylenediamine, 5-methyl-N'-ethyl-N'-(aminocarbonylmethyl)paraphenylenediamine, ...
The process of claim 1 wherein the compound of formula (II) is selected from the group consisting of 2,6-dimethyl-1,4-diaminobenzene, 2,5-dimethyl-1,4-diaminobenzene, 2,3-dimethyl-1,4-diaminobenzene, 2-methoxy-5-methyl-1,4-diaminobenzene, 2-methoxy-5-methyl-4-β-aminoethylamino-1-aminobenzene, 2-methyl-5-chloro-4-β-aminoethylamino-1-aminobenzene, 4,6-dimethoxy-1,3-diaminobenzene, 2,3-dimethyl-4-aminophenol, 2,6-dimethyl-4-aminophenol and ...
In addition to these preferred compounds the compounds of formula (II) which are more particularly preferred are chosen from: 2,6-dimethyl-1,4-diaminobenzene 2,5-dimethyl-1,4-diaminobenzene 2,3-dimethyl-1,4-diaminobenzene 2-methoxy-5-methyl-1,4-diaminobenzene 2-methoxy-5-methyl-4-β-aminoethylamino-1-aminobenzene 2-methyl-5-chloro-4-β-aminoethylamino-1-aminobenzene 4,6-dimethoxy-1,3-diaminobenzene 2,3-dimethyl-4-aminophenol 2,6-dimethyl-4-aminophenol, and ...
The following compounds with formula (IV) may in particular be cited: paraphenylenediamine, paratoluylenediamine, methoxyparaphenylenediamine, chloroparaphenylenediamine, 2,3-dimethylparaphenylenediamine, 2,6-dimethylparaphenylenediamine, 2,6-diethylparaphenylenediamine, 2,5-dimethylparaphenylenediamine, 2,6-dimethyl 5-methoxyparaphenylenediamine, ...
The method of claim 4 wherein said para-phenylenediamine is selected from the group consisting of ... methoxy-para-phenylenediamine, chloro-para-phenylenediamine, 2,6-dimethyl-para-phenylenediamine, 2,5-dimethyl-para-phenylenediamine, 2,3-dimethyl-para-phenylenediamine, 2-methyl-5-methoxy-para-phenylenediamine, 2,6-dimethyl-5-methoxy-para-phenyldiamine, N,N-dimethyl-para-phenyldiamine, ...
, characterized in that the developer is selected from the group consisting of ... 1,4-diamino-2-methylbenzene; 1,4-diamino-2,6-dimethylbenzene; 1,4-diamino-3,5-diethylbenzene; 1,4-diamino-2,5-dimethylbenzene; 1,4-diamino-2,3-dimethylbenzene; 2-chloro-1,4-diaminobenzene; 1,4-diamino-2-(thiophen-2-yl)benzene; 1,4-diamino-2-(thiophen-3-yl)benzene; ...
Nonlimiting examples of suitable aromatic diamines, aminophenols, naphthols, polyhydric phenols and derivatives thereof, respectively, are the following compounds: ... 4-amino-N-ethyl-N-(β-sulfoethyl)aniline, 3-methyl-4-amino-N-ethyl-N-(β-sulfoethyl)aniline, N-(4-aminophenyl)morpholine, N-(4-aminophenyl)piperidine, 2,3-dimethyl-p-phenylenediamine, 2-isopropyl-p-phenylenediamine, N,N-bis-(2-hydroxyethyl)-p-phenylenediamine sulfate, o-aminophenol, ...

  • 16
  • [ 57146-54-0 ]
  • [ 5306-96-7 ]
  • [ 226947-07-5 ]
YieldReaction ConditionsOperation in experiment
61% In methanol (N2); elem. anal.;
  • 17
  • [ 5306-96-7 ]
  • [ 1538-75-6 ]
  • [ 1071519-79-3 ]
YieldReaction ConditionsOperation in experiment
95% In dichloromethane for 4h; Reflux;
  • 18
  • C14H15N3O3S [ No CAS ]
  • [ 5306-96-7 ]
YieldReaction ConditionsOperation in experiment
61% With hydrogenchloride; tin(ll) chloride In methanol; water Reflux;
  • 19
  • [ 57933-83-2 ]
  • [ 5306-96-7 ]
  • C16H20N2O4 [ No CAS ]
YieldReaction ConditionsOperation in experiment
Stage #1: 1,4-diamino-2,3-dimethylbenzene With sodium hydroxide In water; ethyl acetate for 0.166667h; Cooling with ice; Stage #2: Isopropenyl chloroformate In water; ethyl acetate at 0 - 20℃;
  • 20
  • N-benzyl-N-(4-phenylbuta-1,3-diyn-1-yl)-4-methylbenzenesulfonamide [ No CAS ]
  • [ 5306-96-7 ]
  • N-(6-amino-4-benzyl-7,8-dimethylquinolin-2-yl)-N-benzyl-4-methylbenzenesulfonamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
72% With 2-dicyclohexyl(2′,6′-dimethoxybiphenyl)phosphine gold(I)bis(trifluoromethanesulfonyl)imide In dichloromethane at 80℃; for 12h; Inert atmosphere;
Same Skeleton Products
Historical Records

Related Functional Groups of
[ 5306-96-7 ]

Aryls

Chemical Structure| 137-17-7

[ 137-17-7 ]

2,4,5-Trimethylaniline

Similarity: 1.00

Chemical Structure| 18102-21-1

[ 18102-21-1 ]

2,3,6-Trimethylaniline

Similarity: 1.00

Chemical Structure| 2217-45-0

[ 2217-45-0 ]

2,3,4,5-Tetramethylaniline

Similarity: 1.00

Chemical Structure| 1467-35-2

[ 1467-35-2 ]

2,3,4-Trimethylaniline

Similarity: 1.00

Chemical Structure| 767-77-1

[ 767-77-1 ]

2,3,5-Trimethylaniline

Similarity: 1.00

Amines

Chemical Structure| 137-17-7

[ 137-17-7 ]

2,4,5-Trimethylaniline

Similarity: 1.00

Chemical Structure| 18102-21-1

[ 18102-21-1 ]

2,3,6-Trimethylaniline

Similarity: 1.00

Chemical Structure| 2217-45-0

[ 2217-45-0 ]

2,3,4,5-Tetramethylaniline

Similarity: 1.00

Chemical Structure| 1467-35-2

[ 1467-35-2 ]

2,3,4-Trimethylaniline

Similarity: 1.00

Chemical Structure| 767-77-1

[ 767-77-1 ]

2,3,5-Trimethylaniline

Similarity: 1.00