Scholarly article on bis-[2-(4-nitro-benzoyloxy)-ethyl]-disulfide 101732-49-4 from Journal of the American Chemical Society p. 838,840

DOI: 10.1021/ja01537a022

Source and publish data:

Journal of the American Chemical Society p. 838,840 (1958)

Update date:2022-08-05

Topics:

Authors:

Field Field

Lawson Lawson

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

Article abstract of DOI:10.1021/ja01537a022

Full text of DOI:10.1021/ja01537a022

Products guided by the article

Product name:bis-[2-(4-nitro-benzoyloxy)-ethyl]-disulfide

Cas No:101732-49-4

R&D Labs maybe for 101732-49-4

Changzhou Welton Chemical Co., Ltd,

Contact:0086-519-85910828,85920537,85912897

Address:No.8 Jinlong Road, Binjiang Park, Changzhou, Jiangsu, China.
ZhangJiaGang YaRui Chemical Co.,Ltd.

Contact:0512-58360968

Address:China JiangSu Province Zhang Jia Gang City YangShe Oriental Plaza Building 10 B307
Xi'an Costrong Pharmaceutical Co., Ltd.

Contact:029- 68576496

Address:Room 2004,Shuibao Building,No.190,South Erhuan Rd, Yanta District,Xi'an,Shaan Xi,China
ShangHai BMG Chemical Co., Ltd

Contact:+86-13524845543

Address:Room 602, no 291 sikai road shanghai
Shanghai TBBMed Co.,Ltd

website:http://www.tbbmed.com

Contact:86--21-50498136

Address:Room 6002, Building 7-1, No.160 Basheng Road,Pudong Area,Shanghai China

Relevant to this article

One-Pot Electrochemical Nickel-Catalyzed Decarboxylative Sp²-Sp³ Cross-Coupling

Doi:10.1021/acs.orglett.8b04090
(2019)
Pentakis(trifluoromethyl)phenyl, a sterically crowded and electron-withdrawing group: Synthesis and acidity of pentakis(trifluoromethyl) benzene, -toluene, -phenol, and -aniline

Doi:10.1021/jo702513w
(2008)
Copper(II) bromide catalyzed novel preparation of propargylic ethers and sulfides by S_N1-type substitution between propargylic alcohols and alcohols or thiols

Doi:10.1055/s-2007-990951
(2008)
Facile rearrangement of N⁴-(α-aminoacyl)cytidines to N-(4-cytidinyl)amino acid amides

Doi:10.1016/j.tetlet.2008.02.015
(2008)
Doi:10.1002/hlca.19410240191
(1941)
Total Synthesis of (+)-MPC1001B

Doi:10.1002/anie.201507830
(2016)

Article Doi

DOI: 10.1021/ja01537a022