Carcinogenic azo dyes. XVIII. Syntheses of azo dyes related to 3'-hydroxy-methyl-4-(dimethylamino)azobenzene, a new potent hepatocarcinogen

DOI: 10.1248/cpb.29.1439

Source and publish data:

Chemical and Pharmaceutical Bulletin p. 1439 - 1442 (1981)

Update date:2022-08-03

Topics:

Authors:

Mori Mori

Niwa Niwa

Toyoshi Toyoshi

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

Article abstract of DOI:10.1248/cpb.29.1439

Full text of DOI:10.1248/cpb.29.1439

NII-Electronic Library Service

Products guided by the article

Product name:N-[4-(3-Hydroxymethyl-phenylazo)-phenyl]-N-methyl-acetamide

Cas No:78914-76-8

R&D Labs maybe for 78914-76-8

Phantom-pharma

Contact:

Address:
Hisyntech Corporation Limited

Contact:0086-22-23410962

Address:17-201, Ningfuli, Shuishanggongyuandong road,Nankai district, Tianjin, China
Lyrin Industrial Corporation Limited

Contact:86-731-82571800

Address:Rm 2408,Asia Economy International Building,Shaoshan Road South,Yuhua District,Changsha,Hunan,China
Nantong LiKai Chemical Co.,Ltd

Contact:+86-513-89068669

Address:Jincheng Science Park
Rely Chemicals Ltd.

Contact:+86-518-81061113

Address:No. 8 Lingzhou Road, Lianyungang, Jiangsu, China

Relevant to this article

Doi:10.1021/ja01315a042
(1935)
3,4,9,9a-Tetrahydro-1,4-ethano-3,4a-(iminoethano)-4aH-carbazol-2(1H)-one Derivatives and N,3-Disubstituted 3,3a,4,4a,10,10a-Hexahydro-3a-hydroxy-2-oxo-1,9b:4,10-diethanoimidazo<4,5-b>carbazole-5(2H)-carboxamides

Doi:10.1021/jo00337a021
(1981)
Synthesis of alkyl glycosides using trialkyl borates

Doi:10.3987/COM-00-8899
(2000)
Bifunctional catalysis of ester aminolysis - A computational and experimental study

Doi:10.1002/jlac.199619961003
(1996)
HETERODIENE SYNTHESES-XXIV CHANGES IN THE REACTIVITY OF 2-OXOINDOLIN-3-YLIDENE DERIVATIVES WITH ETHYLVINYLETHER INDUCED BY ELECTRON-WITHDRAWING GROUPS. THE IMPORTANCE OF THE LUMO COEFFICIENTS

Doi:10.1016/S0040-4020(01)98944-6
(1981)
Three-Component Ring-Opening Reactions of Cyclic Ethers, α-Diazo Esters, and Weak Nucleophiles under Metal-Free Conditions

Doi:10.1021/acs.joc.8b02091
(2018)

Article Doi