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13296-94-1

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13296-94-1 Usage

Chemical Properties

Yellow solid

Uses

2-Bromo-4-nitroaniline is used as a reagent in the synthesis of novel tetrahydrothienopyridopyrimidine derivatives which exhibit antibacterial and antifungal activity against a variety of microorganisms in vitro. Also used as a reagent in synthesis of dialkylimidazole inhibitors of Trypanosoma cruzi sterol 14α-demethylase as anti-Chagas disease agents.

Check Digit Verification of cas no

The CAS Registry Mumber 13296-94-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,2,9 and 6 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13296-94:
(7*1)+(6*3)+(5*2)+(4*9)+(3*6)+(2*9)+(1*4)=111
111 % 10 = 1
So 13296-94-1 is a valid CAS Registry Number.
InChI:InChI=1/C6H5BrN2O2/c7-5-3-4(9(10)11)1-2-6(5)8/h1-3H,8H2

13296-94-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Bromo-4-nitroaniline

1.2 Other means of identification

Product number -
Other names 2-bromo-4-nitroaniline

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:13296-94-1 SDS

13296-94-1Relevant articles and documents

An engineered linker capable of promoting on-resin reactions for microwave-assisted solid-phase organic synthesis

Sun, Li-Ping,Dai, Wei-Min

, p. 7255 - 7258 (2006)

An active link: A diglycine-containing linker (cat·linker) was fabricated on Rink amide resin for dual functions: a) attachment of a scaffold and b) capture of metal ions for promoting on-resin reactions (see picture). The metal-catching feature of the li

Stereospecific 1,3-Aminobromination of Donor–Acceptor Cyclopropanes

Das, Saikat,Daniliuc, Constantin G.,Studer, Armido

, p. 11554 - 11558 (2017)

Sn(OTf)2-catalyzed 1,3-aminobromination of donor–acceptor cyclopropanes with various sulfonyl amides or electron-poor anilines and N-bromosuccinimide is reported. These experimentally straightforward reactions occurred with complete regio- and

Rhodium-Catalyzed Synthesis and Optical Properties of Silicon-Bridged Arylpyridines

Shintani, Ryo,Misawa, Nana,Takano, Ryo,Nozaki, Kyoko

, p. 2660 - 2665 (2017)

A convergent and regioselective synthesis of silicon-bridged 4-arylpyridines has been developed through a rhodium-catalyzed [2+2+2] cycloaddition of silicon-containing diynes with nitriles. The absorption and emission properties of these compounds have be

DEOXYNOJIRIMYCIN DERIVATIVES AS GLUCOSIDASE INHIBITORS

-

Paragraph 0716, (2022/01/22)

The present invention relates to novel iminosugars and their use as glucosidase inhibitors. The present inventors discovered that certain deoxynojirimycin derivatives may be effective in inhibiting glucosidases. In particular, such deoxynojirimycin derivatives may be useful for treating a disease or condition in which inhibition of glucosidase may play an important role.

A Practical Procedure for Regioselective Bromination of Anilines

Takahashi, Yusuke,Seki, Masahiko

, p. 1828 - 1832 (2021/04/15)

A highly practical procedure for the preparation of bromoanilines by using copper-catalyzed oxidative bromination has been developed. Treatment of free anilines with readily available NaBr and Na 2S 2O 8in the presence of a catalytic amount of CuSO 4·5H 2O enabled regioselective bromination.

Cu-mediated selective bromination of aniline derivatives and preliminary mechanism study

Zhao, Hong-Yi,Yang, Xue-Yan,Lei, Hao,Xin, Minhang,Zhang, San-Qi

supporting information, p. 1406 - 1415 (2019/05/01)

A simple and efficient bromination of aniline, aniline derivatives, and analogs have been developed. Forty three examples were given and the highest yield reached was 98%. Different substrates including substituted aniline, pyridin-amine, N-substituted aniline, N,N-disubstituted aniline, N-phenyl-amide, N-phenyl-sulfonamide, and nitrogen-containing heterocycles were all reactive and selectively generated desired bromo-products. The method can be applied to synthesize drug intermediate and quinoxaline derivatives.

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