Scholarly article on dimethyl-((1RS,2RS)-1-methyl-2-phenyl-propyl)-amine 105254-12-4 from Journal of the American Chemical Society p. 5740,5743

DOI: 10.1021/ja01651a035

Source and publish data:

Journal of the American Chemical Society p. 5740,5743 (1954)

Update date:2022-08-04

Topics:

Authors:

Cram Cram

McCarty McCarty

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

Article abstract of DOI:10.1021/ja01651a035

Full text of DOI:10.1021/ja01651a035

Products guided by the article

Product name:dimethyl-((1RS,2RS)-1-methyl-2-phenyl-propyl)-amine

Cas No:105254-12-4

R&D Labs maybe for 105254-12-4

SINO Industries Company Limited(expird)

Contact:86-29-85369724

Address:No.111, Jiefang Road, Xi’an, China
KODI CHEMICAL CO., LTD

Contact:021

Address:Pudong
Goldwills Pharmaceuticals Co., Ltd.

Contact:0916-2237889 13991621155

Address:North Suburb of Hanzhong city, Shaanxi Province
CHEM PLUS

Contact:0027-717-456976

Address:2ND FLOOR, 325 VAUSE ROAD, OVERPORT, 4001, SOUTH AFRICA
Jiangsu Willing Bio-Tech Co ltd

website:http://www.willingbio.com/

Contact:+86 18796908173

Address:No 18 Guoqiao Road

Relevant to this article

Determination of the absolute configuration of the cytotoxic natural product pericosine D

Doi:10.1016/j.tetasy.2008.06.008
(2008)
Practical Synthesis of D- and L-2-Cyclopentenone and their Utility for the Synthesis of Carbocyclic Antiviral Nucleosides against Orthopox Viruses (Smallpox, Monkeypox, and Cowpox Virus)

Doi:10.1021/jo034999v
(2003)
Aromatization via a dibromination-double dehydrobromination sequence: A facile and convenient synthetic route to 2,6-bis(trifluoroacetyl)phenols

Doi:10.1055/s-2008-1067080
(2008)
Benzenesulfonamide derivatives of 2-substituted 4H-3,1-benzoxazin-4- ones and benzthiazin-4-ones as inhibitors of complement C1r protease

Doi:10.1016/S0960-894X(99)00095-5
(1999)
Doi:10.1016/0040-4020(66)80148-5
(1966)
Characterization of metabolites of fungicidal cymoxanil in a sensitive strain of Botrytis cinerea

Doi:10.1021/jf8010917
(2008)

Article Doi

DOI: 10.1021/ja01651a035