261661
5-Methyl-2-nitroaniline
95%
Synonym(s):
6-Nitro-m-toluidine
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
Linear Formula:
CH3C6H3(NO2)NH2
CAS Number:
Molecular Weight:
152.15
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
95%
form
powder
mp
110-111 °C (lit.)
functional group
nitro
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 Statements
Precautionary Statements
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
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service