Scholarly article on all-trans-5,6-dihydro-β-carotene 2790-54-7 from Journal of the American Chemical Society p. 1528,1529, 1531

DOI: 10.1021/ja01248a026

Source and publish data:

Journal of the American Chemical Society p. 1528,1529, 1531 (1943)

Update date:2022-08-05

Topics:

Authors:

Polgar Polgar

Zechmeister

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

Article abstract of DOI:10.1021/ja01248a026

Full text of DOI:10.1021/ja01248a026

Products guided by the article

Product name:all-trans-5,6-dihydro-β-carotene

Cas No:2790-54-7

R&D Labs maybe for 2790-54-7

Shanghai Sunwise Chemical Co., Ltd

website:http://www.sunwisechem.com

Contact:86-021-33883180

Address:Room 10E, Building G, Westlink Center, No. 2337 Gudai Road, Minhang District, Shanghai, China PC: 201100
Laizhou City Laiyu Chemical CO.,Ltd

Contact:+86-535-2719337/2719339

Address:Chenggang road zhuyou laizhou City Shangdong China
Hubei Honch Pharmaceutical Co.,Ltd

Contact:86-713-7222018

Address:Li Shizhen Pharmaceutical Industry park, Qichun County, Hubei Province,China
Beijing Apis Biotechnology Co., Ltd.

Contact:86-010-67856775-8551

Address:NO.4PUHUANGYU ROAD,FENTAI DISTRICT, BEIJING, CHINA
Pale Palm Imex

Contact:+36(21)2523420

Address:Head office: 1102 Budapest, SZENT LASZLO TER 24/B. 1/1., HUNGARY / CHINA

Relevant to this article

Doi:10.1139/v70-308
(1970)
Doi:10.1021/ja00864a022
(1962)
Selective formation of substituted pyridines from two different alkynes and a nitrile: Novel coupling reaction of azazirconacyclopentadienes with alkynes [8]

Doi:10.1021/ja000474y
(2000)
Effect of polymethylene and phenylene linking groups on the DNA cleavage specificity of distamycin-linked hydroxamic acid-vanadyl complexes

Doi:10.1248/cpb.48.603
(2000)
A novel assembly of substituted pyrroles by acid-catalyzed sequential three-component reaction of amines, alkynoates, and 1,2-diaza-1,3-dienes

Doi:10.1002/adsc.201100094
(2011)
Synthesis and antibacterial activity of four natural chalcones and their derivatives

Doi:10.1016/j.tetlet.2019.151165
(2019)

Article Doi

DOI: 10.1021/ja01248a026