2-Amino-4-methylbenzonitrile

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2-Amino-4-methylbenzonitrile Basic information
Product Name:2-Amino-4-methylbenzonitrile
Synonyms:4-Methyl-2-aminobenzonitrile;2-AMINO-4-METHYLBENZONITRILE;2-Cyano-5-methylaniline, 3-Amino-4-cyanotoluene, 6-Cyano-m-toluidine;2-Cyano-5-methylaniline, 3-Amino-4-cyanotoluene;Benzonitrile, 2-aMino-4-Methyl-;3-Amino-4-cyanotoluene 2-Cyano-5-methylaniline 6-Cyano-m-toluidine;2-Amino-4-methylbenzonitrile >;2-Cyano-5-methylaniline
CAS:26830-96-6
MF:C8H8N2
MW:132.16
EINECS:248-020-0
Product Categories:Aromatic Nitriles;Amines;Phenyls & Phenyl-Het;Nitrile;Phenyls & Phenyl-Het;C8 to C9;Cyanides/Nitriles;Nitrogen Compounds
Mol File:26830-96-6.mol
2-Amino-4-methylbenzonitrile Structure
2-Amino-4-methylbenzonitrile Chemical Properties
Melting point 92-95 °C (lit.)
Boiling point 150-152 °C(Press: 15 Torr)
density 1.10±0.1 g/cm3(Predicted)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
solubility soluble in Methanol
pka1.94±0.10(Predicted)
form Powder
color Light yellow to Yellow to Orange
InChI1S/C8H8N2/c1-6-2-3-7(5-9)8(10)4-6/h2-4H,10H2,1H3
InChIKeyLGNVAEIITHYWCG-UHFFFAOYSA-N
SMILESCc1ccc(C#N)c(N)c1
CAS DataBase Reference26830-96-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,T
Risk Statements 20/21/22-36/37/38
Safety Statements 26-36-36/37
RIDADR 3439
WGK Germany 3
Hazard Note Toxic
HazardClass 6.1
PackingGroup III
HS Code 29269090
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
2-Amino-4-methylbenzonitrile Usage And Synthesis
Chemical Propertieswhite to light yellow crystal powder
Uses2-Amino-4-methylbenzonitrile was used in the synthesis of:
  • 7-methyl-4-(phenylamino)quinazoline-2(1H)-selone
  • racemic aminoquinolines, potential acetylcholinesterase (AChE) inhibitors
Synthesis
4-Methyl-2-nitrobenzonitrile

26830-95-5

2-Amino-4-methylbenzonitrile

26830-96-6

a) Synthesis of 2-amino-4-methylbenzonitrile 4-Methyl-2-nitrobenzonitrile (4.9 g, 30 mmol) was mixed with 10% palladium-carbon catalyst (500 mg) in 1,4-dioxane (60 mL), and the reaction was stirred overnight under a hydrogen atmosphere (balloon pressurized). Upon completion of the reaction, the catalyst was removed by diatomaceous earth filtration and the filtrate was concentrated under reduced pressure to give the crude product. The crude product was further purified by fast column chromatography (eluent: dichloromethane) to afford 2-amino-4-methylbenzonitrile as a light yellow solid (3.3 g, 83% yield). 1H-NMR (300 MHz, CDCl3) δ 7.26 (d, J = 8.3 Hz, 1H), 6.56 (s, 1H), 6.55 (s, 1H), 4.32 (br s, 2H), 2.29 (s, 3H).

References[1] Chemical Communications, 2011, vol. 47, # 31, p. 8808 - 8810
[2] Journal of the Chemical Society, Perkin Transactions 2, 2001, # 2, p. 214 - 228
[3] Patent: US5891909, 1999, A
[4] Patent: EP906091, 2006, B1. Location in patent: Page/Page column 46
[5] Journal fuer Praktische Chemie (Leipzig), 1889, vol. <2> 40, p. 12
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