Scholarly article on 4-(3-nitro-phenylazo)-benzonitrile 106037-98-3 from Journal of the American Chemical Society p. 3274,3275

DOI: 10.1021/ja01522a030

Source and publish data:

Journal of the American Chemical Society p. 3274,3275 (1959)

Update date:2022-08-04

Topics:

Authors:

Yeh Yeh

Jaffe Jaffe

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1021/ja01522a030

Full text of DOI:10.1021/ja01522a030

Products guided by the article

Product name:4-(3-nitro-phenylazo)-benzonitrile

Cas No:106037-98-3

R&D Labs maybe for 106037-98-3

Zhaodu Fine Chemical Plant

Contact:86-310-8067016

Address:East Fuhua Road,Tiexi Chemical Industrial Estate,Hebei,China
Chongqing Shuangfeng Chemical Co.,Ltd

Contact:+86-23-49850156

Address:No.663,xuanhua Rd,yongchuan,chongqing,China
Yuan Shi(SuQian)Biotechnology Co.,Ltd

website:http://www.yuanshibio.com

Contact:+86-527-84226672

Address:jiangsu suqian
Ningbo Inno Pharmchem Co., Ltd.

Contact:86-574-87319282

Address:6F-5,NO.163 RUIQING RD.,NINGBO 315000 CHINA
Lonzeal Pharmaceuticals Co., Ltd.

website:http://www.lonzeal.com

Contact:+86-13381011962

Address:RM 801, Yue MOMA, No. 26 Anningzhuang Rd. Haidian District, Beijing, China

Relevant to this article

Doi:10.1021/jm00340a017
(1963)
Synthesis of thiazolo[4,5-d]pyridines

Doi:10.1055/s-2008-1067152
(2008)
SYNTHESIS OF SUBSTITUTED TETRAHYDROFURANS AND TETRAHYDROPYRANS. 2. STEREOCONTROLLED ACID-CATALYZED CYCLIZATIONS

Doi:10.1016/S0040-4039(00)84411-1
(1986)
Cyclophanes of perylene tetracarboxylic diimide with different substituents at bay positions

Doi:10.1002/chem.200800136
(2008)
Substituted 3-((Z)-2-(4-nitrophenyl)-2-(1H-tetrazol-5-yl) vinyl)-4H-chromen-4-ones as novel anti-MRSA agents: Synthesis, SAR, and in-vitro assessment

Doi:10.1016/j.bmcl.2008.07.007
(2008)
On the Stereo- and Regioselectivity of Molybdenum-Catalyzed Allylic Alkylations. Stereocontrolled Approach to Quaternary Carbons and Tandem Alkylation-Cycloaddition

Doi:10.1021/ja00348a068
(1983)

Article Doi

DOI: 10.1021/ja01522a030