Scholarly article on 2-chloro-pentanedioic acid 1369533-83-4 from Bulletin of the Chemical Society of Japan p. 1264,1265

DOI: 10.1246/bcsj.36.1264

Source and publish data:

Bulletin of the Chemical Society of Japan p. 1264,1265 (1963)

Update date:2022-08-04

Topics:

Authors:

Saotome Saotome

Yamazaki

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

Article abstract of DOI:10.1246/bcsj.36.1264

Full text of DOI:10.1246/bcsj.36.1264

Products guided by the article

Product name:2-chloro-pentanedioic acid

Cas No:1369533-83-4

R&D Labs maybe for 1369533-83-4

SHIFANG SUHONG CHEMICAL CO.,LTD

Contact:+86-838-2224563

Address:Room 1207 Zongchen Sunshine No.128 Taishan South Road,Deyang City,Sichuan China
Weifang Arylchem Chemical Co., LTD

Contact:86-536-5217866

Address:Development Zone, Shouguang, Shandong Province
Taixing Shenfeng Chemical Co., Ltd.

Contact:+86-523-87117033, 87117666

Address:4# Yinsanlu, Huangqiao town, Taixing, Jiangsu, China.
Yangzhou Siyu Chemical Co.,Ltd.

Contact:+86-514-87325867 13358126196

Address:Room 620 Exposition Pavilion，No. 98 Huaihai Road,Guangling District，Yangzhou City, Jiangsu Province
ShanDong XinDa Chemical CO.,LTD(expird)

Contact:086-0311-87580543

Address:No.168, High Technology Development Zone Jinan Shandong China

Relevant to this article

Hybrids of privileged structures benzothiazoles and pyrrolo[2,1-c] [1,4]benzodiazepin-5-one, and diversity-oriented synthesis of benzothiazoles

Doi:10.1016/j.ejmech.2012.01.014
(2012)
Design, synthesis, biological evaluation, and molecular modeling studies of quinoline-ferulic acid hybrids as cholinesterase inhibitors

Doi:10.1016/j.bioorg.2019.103310
(2019)
Synthesis and biological evaluation of novel AM80 derivatives as antileukemic agents

Doi:10.1007/s00044-012-0019-9
(2013)
Enantioselective synthesis of 3,4-dihydropyran derivatives via organocatalytic Michael reaction of α,β-unsaturated enones

Doi:10.1021/jo3001047
(2012)
Transition Metal-Free Synthesis of 3-Alkynylpyrrole-2-carboxylates via Michael Addition/Intramolecular Cyclodehydration

Doi:10.1002/adsc.201501073
(2016)
Inhibitory effect of 2-(E-2-alkenoylamino)ethyl alkyl sulfides on gastric ulceration in rats. II. Structure and activity relationships of 2(E-n or Z-n-decenoylamino)ethyl alkyl sulfides

Doi:10.1248/cpb.39.1546
(1991)

Article Doi

DOI: 10.1246/bcsj.36.1264

Source and publish data: