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Merck
CN

261661

5-Methyl-2-nitroaniline

95%

Synonym(s):

6-Nitro-m-toluidine

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About This Item

Linear Formula:
CH3C6H3(NO2)NH2
CAS Number:
578-46-1
Molecular Weight:
152.15
NACRES:
NA.22
PubChem Substance ID:
24855829
UNSPSC Code:
12352100
EC Number:
209-423-7
MDL number:
MFCD00007814
Assay:
95%
Form:
powder

Key Documents

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Product Name

5-Methyl-2-nitroaniline, 95%

InChI key

IGDYNWKWXUCIJB-UHFFFAOYSA-N

InChI

1S/C7H8N2O2/c1-5-2-3-7(9(10)11)6(8)4-5/h2-4H,8H2,1H3

SMILES string

Cc1ccc(c(N)c1)[N+]([O-])=O

assay

95%

form

powder

mp

110-111 °C (lit.)

functional group

nitro

Quality Level

100

Gene Information

rat ... Nos1(24598)

Related Categories

Application

5-Methyl-2-nitroaniline has been used in the preparation of N-(5-methyl-2-nitrophenyl)-4-[N-(pyridin-3-ylmethoxy carbonyl)aminomethyl]benzamide.

signalword

Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 2 - STOT RE 2

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
STBF4836V
S27275V
S27275
10730HD
12004CB

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T Suzuki et al.
Journal of medicinal chemistry, 42(15), 3001-3003 (1999-07-30)
Newly synthesized benzamide derivatives were evaluated for their inhibitory activity against histone deacetylase. The structure of these derivatives was unrelated to the known inhibitors, and IC(50) values of the active compounds were in the range of 2-50 microM. Structure-activity relationship

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