Scholarly article on 1-cyclohexyl-3-diethylamino-2-methyl-1-phenyl-propan-1-ol 110436-78-7 from Journal of the American Chemical Society p. 718,719

DOI: 10.1021/ja01158a018

Source and publish data:

Journal of the American Chemical Society p. 718,719 (1950)

Update date:2022-07-29

Topics:

Authors:

Ruddy Ruddy

Buckley Buckley

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

Article abstract of DOI:10.1021/ja01158a018

Full text of DOI:10.1021/ja01158a018

Products guided by the article

Product name:1-cyclohexyl-3-diethylamino-2-methyl-1-phenyl-propan-1-ol

Cas No:110436-78-7

R&D Labs maybe for 110436-78-7

Jiangsu Mingchem Corporation

website:http://www.mingchem.com/en/index

Contact:0519-85170101-802

Address:Fifth Floor,B of Beihua Buliding,520 Road of Science and Education City,Changwu middle road NO.801,Wujin District,Changzhou,Jiangsu province
Langchem

Contact:+86+21-58956006 15800617331

Address:402 Room, 150# Cailun Road, Zhangjiang high tech park, Shanghai
Wuhan Soleado Technology Co.,Ltd.

Contact:86-2783341481 18971291927

Address:RM2405 Unit 1 Builing 1, Taiyin Tower, Changqing Road,Wuhan China
Beijing Mesochem Technology Co.,LTD

website:http://www.mesochem.com

Contact:0086-10-57862036

Address:2301, Floor 23, Building 9 Lippo Plaza, Yard 8 Ronghua Middle Road, ETDZ, Beijing, China
Nanjing Vincero International Trading Co.,Ltd

Contact:8618936897229

Address:NO.68, ZhuShan Road, JiangNing WanDa Plaza, Building E Room 1703

Relevant to this article

Tandem oxidative amidation of benzyl alcohols with amine hydrochloride salts catalysed by iron nitrate

Doi:10.1016/j.tetlet.2013.07.005
(2013)
AN ASYMMETRIC HYDROGEN EQUIVALENT: USE OF THE 1-NAPHTHYLPHENYLMETHYLSILYL GROUP IN THE PREPARATION OF OPTICALLY ACTIVE ALLYL ALCOHOLS AND (S) 1-PHENYL-1,2-BUTADIENE.

Doi:10.1016/S0040-4039(00)80295-6
(1988)
A study of chiral oxazoline ligands with a 1,2,4-triazine and other six-membered aza-heteroaromatic rings and their application in Cu-catalysed asymmetric nitroaldol reactions

Doi:10.1016/j.tetasy.2014.10.001
(2014)
An efficient and general method for the reformatsky-type reaction of chlorodifluoromethyl ketones with carbonyl compounds giving α,α-difluoro-β-hydroxy ketones¹)

Doi:10.1246/bcsj.63.428
(1990)
Doi:10.1016/0040-4020(65)80025-4
(1965)
Catechuic acid and ethyl 2,4,5-trihydroxybenzoate from d-glucose

Doi:10.1016/j.carres.2009.02.002
(2009)

Article Doi

DOI: 10.1021/ja01158a018