Scholarly article on 2-Butanol, 4-chloro- 2203-34-1 from Journal of the American Chemical Society p. 1791 - 1795

DOI: 10.1021/ja01063a028

Source and publish data:

Journal of the American Chemical Society p. 1791 - 1795 (1964)

Update date:2022-07-30

Topics:

Authors:

Brown,H.C.

Keblys,K.A.

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

Article abstract of DOI:10.1021/ja01063a028

Full text of DOI:10.1021/ja01063a028

Products guided by the article

Product name:2-Butanol, 4-chloro-

Cas No:2203-34-1

R&D Labs maybe for 2203-34-1

Shaanxi HuaTai Bio-fine chemical company Ltd

Contact:86-029-87862197

Address:No. 5, 3rd Floor, 29 Yanta North Road, Beilin Dist.
Zhejiang Chemicals Import & Export Corporation (ZHECHEM)

Contact:+86-571-87046953

Address:No. 37, Qingchun Road
Luojiang Chenming Biological Products Co

Contact:+86 15000297032

Address:GROUP NO.4, HE SHENG VILLAGE, PANLONG TOWN,
He Bei Shun Er Chemical Co., LTD.

Contact:86-0311-86996932/86860168

Address:No 18,North street
Nanjing HuiBaiShi Biotechnology Co.,Ltd.

Contact:+86 (25)58745219

Address:No.606 Ningliu Road,LiuHe District.

Relevant to this article

Focused library approach for identification of new N-acylphenylalanines as VCAM/VLA-4 antagonists.

Doi:10.1016/S0960-894X(02)00201-9
(2002)
Novel discotic mesogen: Synthesis and liquid crystalline behavior of TAAB (tetrabenzo[b,f,j,n][1,5,9,13]tetraazacyclohexadecine) derivatives with long alkoxy chains

Doi:10.1039/a808739c
(1999)
Synthesis and characterization of N-glucosylated dithiadiazepine derivatives through carbon-sulfur bond formation

Doi:10.1515/hc-2015-0093
(2015)
Synthesis and biological evaluation of novel heterocyclic ionone-like derivatives as anti-inflammatory agents

Doi:10.1016/j.bmc.2006.04.007
(2006)
Isolation of the reactive intermediate in palladium-catalysed coupling of secondary phosphine-boranes with aryl halides

Doi:10.1039/a807830k
(1999)
Synthesis of thieno[2,3-b][1,5]benzoxazepine derivatives

Doi:10.1002/jhet.5570390124
(2002)

Article Doi

DOI: 10.1021/ja01063a028