<Suppliers Price>

2-Amino-4-methylbenzonitrile

Names

[ CAS No. ]:
26830-96-6

[ Name ]:
2-Amino-4-methylbenzonitrile

[Synonym ]:
Benzonitrile, 2-amino-4-methyl-
2-Amino-4-methylbenzonitrile
4-methylanthranilonitrile
6-Cyano-m-toluidine
2-amino-4-methyl-benzonitrile
4-Methyl-2-nitro-benzonitrile
EINECS 248-020-0
4-METHYL-2-AMINOBENZONITRILE
MFCD00173706
2-Cyano-5-methylaniline
5-methyl-2-cyanoaniline
2-amino-4-methylbenzenecarbonitrile
3-Amino-4-cyanotoluene
2-Amino-4-methyl-benzonitril

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
301.2±30.0 °C at 760 mmHg

[ Melting Point ]:
92-95 °C(lit.)

[ Molecular Formula ]:
C8H8N2

[ Molecular Weight ]:
132.163

[ Flash Point ]:
136.0±24.6 °C

[ Exact Mass ]:
132.068741

[ PSA ]:
49.81000

[ LogP ]:
1.86

[ Vapour Pressure ]:
0.0±0.6 mmHg at 25°C

[ Index of Refraction ]:
1.576

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302 + H312 + H332-H315-H319-H335

[ Precautionary Statements ]:
P261-P280-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xn:Harmful;

[ Risk Phrases ]:
R20/21/22;R36/37/38

[ Safety Phrases ]:
S26-S36-S36/37

[ RIDADR ]:
3439

[ WGK Germany ]:
3

[ Packaging Group ]:
III

[ Hazard Class ]:
6.1

[ HS Code ]:
2926909090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2926909090

[ Summary ]:
HS:2926909090 other nitrile-function compounds VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0%

Articles

Synthesis, in vitro pharmacology, and molecular modeling of very potent tacrine-huperzine A hybrids as acetylcholinesterase inhibitors of potential interest for the treatment of Alzheimer's disease.

J. Med. Chem. 42(17) , 3227-42, (1999)

Eleven new 12-amino-6,7,10,11-tetrahydro-7, 11-methanocycloocta[b]quinoline derivatives [tacrine (THA)-huperzine A hybrids, rac-21-31] have been synthesized as racemic mixtures and tested as acetylcho...

Synthesis of 4-(Phenylamino) quinazoline-2 (1H)-selones and Diselenides from Isoselenocyanates: Dimroth Rearrangement of an Intermediate. Atanassov PK, et al.

Helv. Chim. Acta 87(7) , 1873-7, (2004)


More Articles


Related Compounds

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.