Scholarly article on Benzenethiol, 3-(methylsulfonyl)- 3814-24-2 from Journal of the American Chemical Society p. 6019,6020, 6022

DOI: 10.1021/ja01119a069

Source and publish data:

Journal of the American Chemical Society p. 6019,6020, 6022 (1953)

Update date:2022-07-29

Topics:

Authors:

Bordwell

Andersen

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

Article abstract of DOI:10.1021/ja01119a069

Full text of DOI:10.1021/ja01119a069

Products guided by the article

Product name:Benzenethiol, 3-(methylsulfonyl)-

Cas No:3814-24-2

R&D Labs maybe for 3814-24-2

Qingdao Kylin Trading Co., Ltd.

Contact:0086-532-68979884/58972912/68972263/65/88171519

Address:Room 2308,A building International Trade Center No.230 Changjiang Middle Road of Qingdao Economic Development Zone,Shandong,China.
Amadis Chemical Co., Ltd.

website:http://www.amadischem.com

Contact:86-571-89925085

Address:Watts Cosine.No.166.Xiangmao Road.
WUXI KINGHAN BIO-MEDICAL&CHEMICAL INC.

Contact:13861062998

Address:Room 1316,No.1619 Huishan Avenue,Wuxi,China
NOVASYNCS CO., LTD

Contact:0512-63006287

Address:no.88.YISHENG Road,etdz-WUJIANG,SUZHOU,CHINA
NINGBO YINLIANG FOREIGN TRADE CO., LTD.

Contact:+86-574-87834016 / 87898057

Address:23F NO.666JINYU ROAD,YINGZHOU DISTRICT,NINGBO.CHINA

Relevant to this article

New functionalized alkenylmagnesium reagents bearing an oxygen function in the β-position. Preparation and reaction of 5-magnesiated-1,3-dioxin-4-one derivatives

Doi:10.1016/S0040-4039(01)01426-5
(2001)
Doi:10.1016/0040-4039(76)80004-4
(1976)
Structural assignment of fluorocyclobutenes by¹⁹F NMR spectroscopy – Comparison of calculated¹⁹F NMR shielding constants with experimental¹⁹F NMR shifts

Doi:10.1002/ejoc.201800482
(2018)
Doi:10.1016/S0022-1139(00)83510-1
(1972)
Synthesis and Anticancer Activity of Some New Fused Pyrazoles and Their Glycoside Derivatives

Doi:10.1002/jhet.3208
(2018)
Design, synthesis, and SAR of embelin analogues as the inhibitors of PAI-1 (plasminogen activator inhibitor-1)

Doi:10.1016/j.bmcl.2014.03.045
(2014)

Article Doi

DOI: 10.1021/ja01119a069