Scholarly article on ETHYL-2,2,2-D3 ALCOHOL 1759-87-1 from Journal of the American Chemical Society p. 2248,2253

DOI: 10.1021/ja00788a025

Source and publish data:

Journal of the American Chemical Society p. 2248,2253 (1973)

Update date:2022-08-11

Topics:

Authors:

Casey Casey

Cyr Cyr

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

Article abstract of DOI:10.1021/ja00788a025

Full text of DOI:10.1021/ja00788a025

Products guided by the article

Product name:ETHYL-2,2,2-D3 ALCOHOL

Cas No:1759-87-1

R&D Labs maybe for 1759-87-1

HANWAYS CHEMPHARM CO.,LIMITED

website:http://www.hanwayschem.com

Contact:+86-18502787239(whatsapp)

Address:18-1-802, Green Garden, Jianghan District, Wuhan 430023, China
Joyochem Co., Ltd.

website:http://www.joyochem.com

Contact:0531-82687558, 0531-82687326

Address:Factory Building 11, Jinan Comprehensive free trade zone, Shandong, China
NINGBO YINLIANG FOREIGN TRADE CO., LTD.

Contact:+86-574-87834016 / 87898057

Address:23F NO.666JINYU ROAD,YINGZHOU DISTRICT,NINGBO.CHINA
Hebei Kangtai Pharmaceutical Co.,Ltd

Contact:+86-0317-3512963

Address:Wugang Road,Mengcun of Cangzhou City,Hebei Province ,China
Jiangxi Province Bethel Pharmaceutical Co., Ltd.

Contact:+86-795-259 3456 ，+86-15957688008 13566650571

Address:Huangjindui Chemical Park， Shanggao County ，Yichun city，Jiangxi Province

Relevant to this article

Synthesis of linear and angular aryl-morpholino-naphth-oxazines, their DNA-PK, PI3K, PDE3A and antiplatelet activity

Doi:10.1016/j.bmcl.2016.10.003
(2016)
Transfer hydrogenation of aldehydes with 2-propanol and Raney nickel

Doi:10.1080/00397910500281028
(2005)
On the reaction of 4-chloromethylene-2,6-di-tert-buthylcyclohexa- 2,5-dien-1-one with P(III) acids esters

Doi:10.1134/S1070363209010307
(2009)
Highly Efficient and Selective Hydrogenation of Aldehydes: A Well-Defined Fe(II) Catalyst Exhibits Noble-Metal Activity

Doi:10.1021/acscatal.6b00436
(2016)
Proposed molecular mechanism for the colloidal nanocatalysis of the hexacyanoferrate III-thiosulfate electron transfer reaction: On the involvement of a Prussian blue analogue complex intermediate

Doi:10.1016/j.jcat.2010.07.002
(2010)
Doi:10.1007/BF00480711
()

Article Doi

DOI: 10.1021/ja00788a025

Source and publish data:

Authors:

Article abstract of DOI:10.1021/ja00788a025

Full text of DOI:10.1021/ja00788a025

Products guided by the article

R&D Labs maybe for 1759-87-1

Relevant to this article

Synthesis of linear and angular aryl-morpholino-naphth-oxazines, their DNA-PK, PI3K, PDE3A and antiplatelet activity

Transfer hydrogenation of aldehydes with 2-propanol and Raney nickel

On the reaction of 4-chloromethylene-2,6-di-tert-buthylcyclohexa- 2,5-dien-1-one with P(III) acids esters

Highly Efficient and Selective Hydrogenation of Aldehydes: A Well-Defined Fe(II) Catalyst Exhibits Noble-Metal Activity

Proposed molecular mechanism for the colloidal nanocatalysis of the hexacyanoferrate III-thiosulfate electron transfer reaction: On the involvement of a Prussian blue analogue complex intermediate