Scholarly article on 2-Methyl-4-phenylamino-3-phenylaminomethyl-but-2-en-1-ol 42836-84-0 from Bulletin of the Chemical Society of Japan p. 1819 - 1822

DOI: 10.1246/bcsj.46.1819

Source and publish data:

Bulletin of the Chemical Society of Japan p. 1819 - 1822 (1973)

Update date:2022-08-04

Topics:

Authors:

Oikawa,E.

Tsubaki,S.

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

Article abstract of DOI:10.1246/bcsj.46.1819

Full text of DOI:10.1246/bcsj.46.1819

Products guided by the article

Product name:2-Methyl-4-phenylamino-3-phenylaminomethyl-but-2-en-1-ol

Cas No:42836-84-0

R&D Labs maybe for 42836-84-0

Changzhou BaoKang Pharmaceutical & Chemical Co., Ltd

Contact:(86) 519-88782201 88784080 88785278

Address:Henglin town, changzhou,Jiangsu
NanJing Rate Biochemicals CO., LTD

Contact:+86-25-84931986

Address:NO. 1 Hongjing Road,Jiangning Science Park,Nanjing,China
Dalian RSD International Trade Co.,Ltd.(expird)

Contact:86-22-60875058 58610575

Address:Wantong International Areas, Hongqiao District, Tianjin, China.China
Fujian Huitian Biological Pharmacy Co., Ltd.

Contact:0086-598-8300831; 8339920

Address:No.46,Taijiang Road,Sanming City,Fujian,China
Guangzhou Shiny Co., Ltd.

website:https://www.sinoshiny.com/products

Contact:+86-20-62802632;62802633

Address:Room 330 GIGCAS Building,No.511 Kehua Street,Tianhe District

Relevant to this article

Single-Pot Synthesis Method of 2-Hydroxybenzylidene-4-[(aza, thio)xanthenyl]anilines and Their Plant Growth Regulator Activity

Doi:10.1134/S1070363219040042
(2019)
Reactivities of 9 phenylxanthylium and 9 phenylthioxanthylium salts in electrophilic and nucleophilic reactions. I. Nitration

Doi:10.1248/cpb.21.1272
(1973)
Doi:10.1246/bcsj.46.1509
(1973)
Reactivity of [Re{(κ³-H(μ-H)B (tim^Me)₂}(CO)₃] (tim^Me = 2-mercapto-1-methylimidazolyl) toward neutral substrates

Doi:10.1021/ic011171n
(2002)
Novel Aryl-Substituted Pyrimidones as Inhibitors of 3-Mercaptopyruvate Sulfurtransferase with Antiproliferative Efficacy in Colon Cancer

Doi:10.1021/acs.jmedchem.1c00260
(2021)
A convenient, general procedure for preparing specifically [3H]-labeled amines. Synthesis of [3H]-meperidine hydrochloride.

Doi:10.1021/jm00262a028
(1973)

Article Doi

DOI: 10.1246/bcsj.46.1819