Scholarly article on 4-benzylsulfanyl-2-dichloromethyl-4-methyl-4H-oxazol-5-one 29099-17-0 from Bulletin of the Chemical Society of Japan p. 2159 - 2161

DOI: 10.1246/bcsj.43.2159

Source and publish data:

Bulletin of the Chemical Society of Japan p. 2159 - 2161 (1970)

Update date:2022-08-05

Topics:

Authors:

Kaneda,A.

Sudo,R. Sudo,R.

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

Article abstract of DOI:10.1246/bcsj.43.2159

Full text of DOI:10.1246/bcsj.43.2159

Products guided by the article

Product name:4-benzylsulfanyl-2-dichloromethyl-4-methyl-4H-oxazol-5-one

Cas No:29099-17-0

R&D Labs maybe for 29099-17-0

Tosta Enterprise Co., Ltd.

Contact:+86-134-5286-9121

Address:Add: Wing Tuck Commercial Centre, 177-183 Wing Lok Street, Hong Kong,
Borun Chemical Co.,Ltd.

Contact:+86-574- 87178138; 87297407

Address:No. 809, Liudingxingzuo, cangsong road, Ningbo, China
Quzhou Aokai Chemical Co., Ltd.

Contact:86-570-3032832

Address:NO.16 , Laodong Road,Quzhou City, Zhejiang Province,China
Shanghai Goyic Pharmaceutical&Chemical Co,. Ltd

Contact:+86-021-60275964

Address:No. 528 ruiqing road
Taizhou Shengxing Chempharm Co.,Ltd

Contact:+86-576-88516600

Address:Yantou Chemical Zone Jiaojiang Taizhou Zhejiang China

Relevant to this article

Conversion of Carbonyl Compounds to Olefins via Enolate Intermediate

Doi:10.1002/cjoc.201800554
(2019)
Optimization of a pyrazolo[1,5-a]pyrimidine class of KDR kinase inhibitors: improvements in physical properties enhance cellular activity and pharmacokinetics.

Doi:10.1016/S0960-894X(02)00827-2
(2002)
Synergistic effect of pyrazoles derivatives and doxorubicin in claudin-low breast cancer subtype

Doi:10.1016/j.biopha.2017.12.062
(2018)
The synthesis of 3,4-dimethoxy-6-morphinanone and isomorphinanone. Spectral inspection of the stereochemistry in cis and trans B/C ring fusion

Doi:10.1248/cpb.32.4670
(1984)
Synthesis and antiviral properties of novel analogues of monophosphate and diphosphate bioactive forms of acyclovir

Doi:10.1016/S0014-827X(00)00046-X
(2000)
A new system for catalytic enantioselective reduction of achiral ketones to chiral alcohols. Synthesis of chiral α-hydroxy acids

Doi:10.1016/S0040-4039(00)94581-7
(1990)

Article Doi

DOI: 10.1246/bcsj.43.2159