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 Cale New Material Co.ltd

Contact:+86-515-88334667/88203550

Address:Zhongshan 3rd Road, Coastal Chemical Industry Park, Yancheng, Jiangsu, China
Shanghai KFSL Pharmaceutical Technology Co.,Ltd.

Contact:+86-21-39971718

Address:859 jiadingchengliu shanghai
Xi'an yuanfar international trade company

website:https://www.yuanfarchemical.com

Contact:86-029-88745613 ext 828

Address:Floor19th ,B Building, Oak Block,No.36 South Fenghui Road, Dev. Zone of High-Tech Ind.,Xi’an, China
Shanghai Mio Chemical Co., Ltd

Contact:0086 21- 64401188-622

Address:16 Floor NO.2 Jiefang Building, No. 4855 Dushi Road, 201100 Shanghai, P.R.China
CGeneTech (Suzhou, China) Co., Ltd.

Contact:+86-512-62956962

Address:Room 101，Bld C11,218 Xinghu Rd.,Suzhou industrial Park

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