Scholarly article on 1-[5-nitro-2-(4-nitro-phenylsulfanyl)-phenyl]-ethanone 412340-12-6 from Journal of the American Chemical Society p. 1925,1928

DOI: 10.1021/ja01200a025

Source and publish data:

Journal of the American Chemical Society p. 1925,1928 (1947)

Update date:2022-08-05

Topics:

Authors:

Amstutz Amstutz

Neumoyer

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

Article abstract of DOI:10.1021/ja01200a025

Full text of DOI:10.1021/ja01200a025

Products guided by the article

Product name:1-[5-nitro-2-(4-nitro-phenylsulfanyl)-phenyl]-ethanone

Cas No:412340-12-6

R&D Labs maybe for 412340-12-6

JinTan Pingsheng Chemical Co.,Ltd

Contact:+86-519-82828200

Address:NO.11Danfengxilu Road,Jintan City,Jiangsu,China
Shanghai agrotree chemical co.,ltd.

Contact:+86-21-50117563

Address:Room 8A,liangfeng building,No.8 dongfang RD.pudong,shanghai,China
Liaoyang hengye Chemical Co., Ltd.

Contact:86-419-5850866

Address:North Old Xiaoxiao Road,Yantai District, Dengta, Liaoyang, Liaoning, China
Xi'an Terra Biochem Co. Ltd.

Contact:0086-29-88315623

Address:S711, Innovation Bldg No.25 Gaoxin 1st Rd, Xian P.R of China 710075
zhuzhou zhongle chemical co. ltd.

Contact:+86-0731 28228409

Address:Zhuzhou, Hunan, China

Relevant to this article

Synthesis, characterization, and theoretical studies on some metallophthalocyanines with octakis phenoxyacetamide substituents

Doi:10.1080/15533174.2012.749897
()
A metal-free, aqueous and general route to 1,5-disubstituted-1,2,3- triazoles: "Reversed regioisomeric" 1,3-dipolar cycloaddition of azides and vinyl sulfones

Doi:10.1055/s-0030-1260306
(2011)
Lewis acid-mediated intramolecular addition of silyl enol ethers to internal unactivated alkynes

Doi:10.1139/v01-134
(2001)
Monobenzylethers of (R,R)-1,2-diphenylethane-1,2-diol as a possible alternative to cyclohexyl-based chiral auxiliaries in the stereoselective reduction of α-ketoesters

Doi:10.1016/S0040-4020(01)01117-6
(2002)
Doi:10.1021/jo00960a026
(1973)
Doi:10.1002/hlca.19640470411
(1964)

Article Doi

DOI: 10.1021/ja01200a025