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261661

Sigma-Aldrich

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
EC Number:
209-423-7
MDL number:
MFCD00007814
UNSPSC Code:
12352100
PubChem Substance ID:
24855829
NACRES:
NA.22

Quality Level

100

Assay

95%

form

powder

mp

110-111 °C (lit.)

SMILES string

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

InChI

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

InChI key

IGDYNWKWXUCIJB-UHFFFAOYSA-N

Gene Information

rat ... Nos1(24598)

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.

Signal Word

Danger

Hazard Classifications

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

Storage Class Code

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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