Scholarly article on 1-Carbomethoxy-2-methyl-trans-4,5-dibrom-cyclohex-1-en 70588-28-2 from Journal of the American Chemical Society p. 2470,2473

DOI: 10.1021/ja00503a037

Source and publish data:

Journal of the American Chemical Society p. 2470,2473 (1979)

Update date:2022-08-05

Topics:

Authors:

Boyd Boyd

Berchtold

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

Article abstract of DOI:10.1021/ja00503a037

Full text of DOI:10.1021/ja00503a037

Products guided by the article

Product name:1-Carbomethoxy-2-methyl-trans-4,5-dibrom-cyclohex-1-en

Cas No:70588-28-2

R&D Labs maybe for 70588-28-2

Shanghai chemrole co.,ltd

Contact:021-50278900

Address:No.6,Room 201 ,Lane 299,bisheng road ,shanghai ,china
Guangzhou Puho Pharmaceutical Technology Co. Ltd.

Contact:86-20-29848035/29848075

Address:No.166, Chaoyang East Road, Panyu District, Guangzhou City, Guangdong Province
QINGDAO DEVELOP chemistry Co.,Limited

Contact:+86-532-85807910

Address:98#Nanjing Road, Qingdao, China 266071
HOST COUNTRY LIMITED

Contact:+852 83038667

Address:Room 1502, 15th Floor, SPA Centre,53-55 Lockhart Road, Wanchai, Hong Kong
SHANDONG ZHANHUA YONGHAO PHARMACEUTICAL TECH.CO.,LTD

Contact:+86-576-88685096

Address:GENGJU VILLAGE NORTH ONE KILOMETER,ZHANHUA DISTRICT,BINZHOU CITY,SHANDONG PROVINCE,CHINA.

Relevant to this article

Studies on fluorinated pyrimidines. II. Synthesis and antitumor activity of 5-fluoro-6-subtituted-5,6-dihydrouracil-5-carboxylic acid derivatives

Doi:10.1248/cpb.30.887
(1982)
An efficient, greener, and solvent-free one-pot multicomponent synthesis of 3-substituted quinazolin-4(3H)ones and thienopyrimidin-4(3H)ones

Doi:10.1016/j.tetlet.2012.05.104
(2012)
Design of potent and specific inhibitors of carboxypeptidases A and B.

Doi:10.1021/bi00575a006
(1979)
Value-added chemicals from biomass-derived furans: radical functionalisations of 5-chloromethylfurfural (CMF) by metal-free ATRA reactions

Doi:10.1039/d1ob00013f
(2021)
An interdisciplinary approach to the design of new structures active at the β-adrenergic receptor. Aliphatic oxime ether derivatives

Doi:10.1021/jm00380a001
(1985)
Synthesis of physanol A and B analogs from β-cytosterol

Doi:10.1007/BF02323289
(1999)

Article Doi

DOI: 10.1021/ja00503a037