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2-AMINO-3-CYANOTOLUENE

Application
Product Name
2-AMINO-3-CYANOTOLUENE
CAS No.
69797-49-5
Chemical Name
2-AMINO-3-CYANOTOLUENE
Synonyms
2-AMINO-3-CYANOTOLUENE;2-Cyano-6-methylaniline;3-methyl-2-Amino-benzonitrile;2-AMINO-3-METHYL-BENZONITRILE;Benzonitrile, 2-aMino-3-Methyl-
CBNumber
CB32452268
Molecular Formula
C8H8N2
Formula Weight
132.16
MOL File
69797-49-5.mol
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2-AMINO-3-CYANOTOLUENE Property

storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
Appearance
Light yellow to brown Solid
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Safety

HS Code 
2926907090
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
A898580
Product name
2-Amino-3-methylbenzonitrile
Packaging
2.5g
Price
$155
Updated
2021/12/16
Biosynth Carbosynth
Product number
FA140141
Product name
2-Amino-3-methylbenzonitrile
Packaging
5G
Price
$160
Updated
2021/12/16
Biosynth Carbosynth
Product number
FA140141
Product name
2-Amino-3-methylbenzonitrile
Packaging
2g
Price
$80
Updated
2021/12/16
AK Scientific
Product number
W7951
Product name
2-Amino-3-methylbenzonitrile
Packaging
1g
Price
$97
Updated
2021/12/16
Matrix Scientific
Product number
119558
Product name
2-Amino-3-methylbenzonitrile
Purity
95+%
Packaging
1g
Price
$144
Updated
2021/12/16
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2-AMINO-3-CYANOTOLUENE Chemical Properties,Usage,Production

Application

3-Amino-2-methylbenzonitrile is an aniline heterocyclic compound mainly used in laboratory organic synthesis processes.

Synthesis

53848-17-2

544-92-3

69797-49-5

The general procedure for the synthesis of 2-amino-3-methylbenzonitrile from 2-bromo-6-methylaniline and cuprous cyanide was as follows: cuprous cyanide (CuCN, 197 mg, 2.2 mmol) was added to an anhydrous N-methylpyrrolidone (NMP, 3 mL) solution of 2-bromo-6-methylaniline (126 μL, 1 mmol). The reaction mixture was placed in a microwave reactor and irradiated at 220 °C for 40 min. Upon completion of the reaction, the mixture was cooled to room temperature and poured into a mixture consisting of ammonia (50% w/v, 10 mL) and ice. Subsequently, the mixture was stirred for 30 min and the target product was extracted with dichloromethane (3 x 20 mL). The organic layers were combined, washed sequentially with water and saturated saline, dried with anhydrous magnesium sulfate (MgSO4), and then concentrated. The crude product was purified by silica gel column chromatography (eluent: 50% ethyl acetate/hexane) to give a brown oil, which was crystallized after standing (128 mg, 96% yield). The structure of the product was confirmed by 1H NMR (400 MHz, DMSO-d6) and mass spectrometry (MS): 1H NMR δ 2.08 (s, 3H), 5.68 (bs, 2H), 6.51-6.55 (t, 1H), 7.17-7.19 (d, 1H), 7.22-7.24 (dd, 1H); MS m/z 133 ([M+H ]+).

References

[1] Patent: US2008/306053, 2008, A1. Location in patent: Page/Page column 60

2-AMINO-3-CYANOTOLUENE Preparation Products And Raw materials

Raw materials

Preparation Products

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