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2-[(3-amino-4-methylphenyl)methyl]benzene-1,3-diamine
- Chemical Name: 2-[(3-amino-4-methylphenyl)methyl]benzene-1,3-diamine
- CAS: 94213-31-7
- Purity: 99%
2-[(3-amino-4-methylphenyl)methyl]benzene-1,3-diamine Good Manufacturer supply High Quality 94213-31-7
- Molecular Formula: C36H30NP2*Cl
- Molecular Weight: 574.041
- Vapor Pressure: 6.44E-09mmHg at 25°C
- Boiling Point: 467.6°Cat760mmHg
- Flash Point: 268.4°C
- PSA： 78.06000
- Density: 1.184g/cm3
- LogP: 4.07600
2-[(3-amino-4-methylphenyl)methyl]benzene-1,3-diamine(Cas 94213-31-7) Usage
|
Chemical Class |
Aromatic amines |
|
Usage |
Manufacturing of dyes, pigments, and pharmaceuticals |
|
Primary Role |
Intermediate in the synthesis of various organic compounds |
|
Biological Target Binding |
Strong binding affinity with certain biological targets |
|
Potential Applications |
Anticancer and antimalarial drugs due to metal ion complex formation |
|
Health Hazards |
Skin and eye irritation, harmful if ingested or inhaled (precautionary handling required) |
|
General Description |
2-[(3-amino-4-methylphenyl)methyl]benzene-1,3-diamine is a chemical compound that belongs to the class of aromatic amines. It has the chemical formula C15H18N2 and is commonly used in the manufacturing of dyes, pigments, and pharmaceuticals. 2-[(3-amino-4-methylphenyl)methyl]benzene-1,3-diamine is primarily used as an intermediate in the synthesis of various organic compounds and is known for its strong binding affinity with certain biological targets. Additionally, 2-[(3-amino-4-methylphenyl)methyl]benzene-1,3-diamine has been studied for its potential application in anticancer and antimalarial drugs due to its ability to form complexes with metal ions. However, it is important to handle this compound with caution, as it may pose health hazards such as skin and eye irritation, and may be harmful if ingested or inhaled. |
InChI:InChI=1/C14H17N3/c1-9-5-6-10(8-14(9)17)7-11-12(15)3-2-4-13(11)16/h2-6,8H,7,15-17H2,1H3
94213-31-7 Relevant articles
Nitrosopersulfide (SSNO-) is a unique cysteine polysulfidating agent with reduction-resistant bioactivity
Bogdándi, Virág,Ditrói, Tamás,Bátai, István Zoárd,Sándor, Zoltán,Minnion, Magdalena,Vasas, Anita,Galambos, Klaudia,Buglyó, Péter,Pintér, Erika,Feelisch, Martin,Nagy, Péter
, p. 1277 - 1294 (2020/11/26)
Aims: The aim of the present study was t...
Probing the mechanism of the PCl5-initiated living cationic polymerization of the phosphoranimine Cl3P=NSiMe3 using model compound chemistry
Blackstone, Vivienne,Lough, Alan J.,Murray, Martin,Manners, Ian
experimental part, p. 3658 - 3667 (2009/09/24)
New insight into the mechanism of the am...
Efficient phosphorus catalysts for the halogen-exchange (Halex) reaction
Lacour, Marie-Agnes,Zablocka, Maria,Duhayon, Carine,Majoral, Jean-Pierre,Taillefer, Marc
supporting information; experimental part, p. 2677 - 2682 (2009/10/20)
New families of monomeric to dendritic, ...
Cyclic sulphur-nitrogen compounds and phosphorus reagents: Part XIII-Reactions of cyclic sulphur-nitrogen chlorides with Ph3P-influences of tetiary base, Et3N and the ring size of the cyclothiazyl chloride on the product formation
Mohan, T.,Senthivel, P.,Rao, M. N. Sudheendra
, p. 961 - 966 (2007/10/03)
Similar to the reactions with S4N3Cl and...
94213-31-7 Process route
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-
C36 H30 NP2 (1+) *C8 H6 ClN2 O2 Te(1-)
-
-
612-23-7
2-nitrobenzyl chloride
-
-
21050-13-5
bis(triphenylphosphine)iminium chloride
| Conditions | Yield |
|---|---|
|
In
acetonitrile;
at 25 ℃;
Equilibrium constant;
|
-
-
603-35-0
triphenylphosphine
-
-
21050-13-5
bis(triphenylphosphine)iminium chloride
-
-
3878-45-3
triphenylphosphine sulfide
| Conditions | Yield |
|---|---|
|
With
S3N2Cl2;
at 140 ℃;
for 5h;
|
0.43 g
68% |
94213-31-7 Upstream products
-
15729-44-9
amino(triphenyl)phosphonium chloride
-
56-23-5
tetrachloromethane
-
17154-23-3
p-nitro-N-(triphenylphosphoranylidene)benzenesulfenamide
-
85071-27-8
2-nitrobenzyl thiocyanate
