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3,6-Dimethyl-2-nitroaniline is an organic compound with the molecular formula C8H10N2O2. It is characterized by the presence of two methyl groups at the 3rd and 6th positions, and a nitro group at the 2nd position of the aniline molecule. 3,6-DIMETHYL-2-NITROANILIN is known for its potential applications in various industries due to its unique chemical properties.

15540-85-9

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15540-85-9 Usage

Uses

Used in Pharmaceutical Industry:
3,6-Dimethyl-2-nitroaniline is used as a reagent for the preparation of quinoxaline-diones, which are potential D-amino acid oxidase inhibitors. These inhibitors play a crucial role in the development of drugs targeting various diseases, including neurodegenerative disorders and certain types of cancer. The compound's ability to form quinoxaline-diones makes it a valuable asset in the pharmaceutical industry for drug discovery and development.

Check Digit Verification of cas no

The CAS Registry Mumber 15540-85-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,5,4 and 0 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 15540-85:
(7*1)+(6*5)+(5*5)+(4*4)+(3*0)+(2*8)+(1*5)=99
99 % 10 = 9
So 15540-85-9 is a valid CAS Registry Number.

15540-85-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,6-dimethyl-2-nitroaniline

1.2 Other means of identification

Product number -
Other names Benzenamine,3,6-dimethyl-2-nitro

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:15540-85-9 SDS

15540-85-9Relevant academic research and scientific papers

Synthesis of ortho-phenylenebis(guanidine) derivatives with potential chirality

Fukuzumi, Masahiro,Nakanishi, Waka,Ishikawa, Tsutomu,Kumamoto, Takuya

, p. 1453 - 1468 (2015/02/19)

We report the synthesis and potential chirality of ortho-phenylenebisguanidines (BGs) with substituents at C(3) and C(6). Guanidinylation of 3,6-disubstituted benzene-1,2-diamines with 2-chloro-4,5-dihydro-1,3-dimethyl-1H-imidazolium chloride gave the corresponding BGs. X-Ray crystallography showed that the two guanidine moieties occupy different faces of the benzene ring, creating potential chirality, although optical resolution of tBu-substituted BG by chiral HPLC failed. However, a methylated acyclic bisguanidinium salt (BGms) was obtained as a chiral crystal with a space group of P212121.

Photocyclisations of Unsaturated 4>Paracyclophanes

Thulin, Bengt,Wennerstroem, Olof

, p. 589 - 596 (2007/10/02)

The photocyclisation of 4>paracyclophanes with one or two unsaturated bridges, compounds 7 and 3, gives 3>(3,6)phenanthrenodiparacyclophane, 8, and 2>(2,13)pentahelicenoparacyclophane, 4, respectively.In contrast, 2

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