Scholarly article on (2E)-3-[(4-methylphenyl)sulfanyl]prop-2-enoic acid 710-38-3 from Journal of the American Chemical Society p. 5311,5313

DOI: 10.1021/ja01576a062

Source and publish data:

Journal of the American Chemical Society p. 5311,5313 (1957)

Update date:2022-08-05

Topics:

Authors:

Truce Truce

Heine Heine

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

Article abstract of DOI:10.1021/ja01576a062

Full text of DOI:10.1021/ja01576a062

Products guided by the article

Product name:(2E)-3-[(4-methylphenyl)sulfanyl]prop-2-enoic acid

Cas No:710-38-3

R&D Labs maybe for 710-38-3

Jiangsu Jiuri Chemical Co.,Ltd.

Contact:+86-519-82118868

Address:Tianwang Town, Jurong City, Jiangsu Province, China
EGBERT CORPORATION

Contact:+86 18616952870

Address:Area
Zhongshan Haihong Medicine Co., Ltd.

Contact:86-0760-86925778 （0）18824993998

Address:A7 building,lianyuan road Torch Hi-tech Industrial Development Zone
NINGBO YINZHOU PRECISE COLOR CO.,LTD.

Contact:86-574-88139809 86-574-83033159

Address:Qiming Road,Yinzhou,Ningbo,China
Shanghai Yurui Biotechnology(Anyang) Pharmaceutical Co., Ltd

Contact:+86-0372-3662335 +86-0372-3661988

Address:hanling industrial park anyang

Relevant to this article

Identification of metabolites of 1-(tetrahydro-2-furanyl)-5-fluorouracil (FT-207) formed in vitro by rat liver microsomes.

Doi:10.1248/cpb.28.1795
(1980)
Tandem [2 + 2] cycloaddition-cycloreversion reactions in highly polar media: A convergent one-pot entry to substituted alkenes and dienes

Doi:10.1016/0040-4039(96)01562-6
(1996)
Structural studies of N-2-(3-picolyl)- and N-2-(4-picolyl)-N′ -tolylthioureas

Doi:10.1023/A:1021136508168
(2002)
A rapid and convenient method for preparing acylhydrazines from acyldiazenes

Doi:10.1002/jccs.200400125
(2004)
Synthesis of O- and C-glycosides derived from β-(1,3)-d-glucans

Doi:10.1016/j.carres.2013.07.007
(2013)
Palladium-catalyzed ortho-olefination of 2-arylpyrrolidines: A tool for increasing structural complexity in nitrogen heterocycles

Doi:10.1016/j.tet.2018.05.076
(2018)

Article Doi

DOI: 10.1021/ja01576a062