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

Hebei Shengang Trading Co.,Ltd(expird)

Contact:0086-0311-80690849

Address:Gaozhu building 1509, No.10 North Zhonghua Main Street, Shijiazhuang city, Hebei Province，China.
Shandong Dayi Chemical Co., Ltd.

website:http://www.dayi.com.cn

Contact:+86- 535-7388728. 15306386031

Address:No 1 Danya west road, Laiyang City, Shandong province
Yurui(Shanghai)Chemical Co.,Ltd

Contact:0086 21-50456736

Address:No.3188 Xiupu Road,Shanghai
Hangzhou yi lu biont technology Co., LTD

Contact:+86-571-88152630

Address:Hangzhoushi HuafengRoad Yicheng3Building1001room.
Xiamen Huasing Chemicals Co.Ltd.

Contact:0086-592-6228397

Address:NO.24, Xinglin North 2nd Road,Jimei district

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