Scholarly article on 2-chloromethyl-3,5,6-trimethyl-hydroquinone 854693-15-5 from Journal of the American Chemical Society p. 524,527

DOI: 10.1021/ja01255a015

Source and publish data:

Journal of the American Chemical Society p. 524,527 (1942)

Update date:2022-08-05

Topics:

Authors:

Smith Smith

Carlin Carlin

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

Article abstract of DOI:10.1021/ja01255a015

Full text of DOI:10.1021/ja01255a015

Products guided by the article

Product name:2-chloromethyl-3,5,6-trimethyl-hydroquinone

Cas No:854693-15-5

R&D Labs maybe for 854693-15-5

Baoji Kano Phytochem Technology Co.,Ltd

Contact:86-917-3816534

Address:No.4 Huoju Road,High-Tech Development Zone
Jinan Great Chemical Co.,Ltd.

Contact:+86-531-58668191 58668193 58668196 58661173

Address:No 55,Beixiaoxinzhuang West Street,Jinan City, Shandong Province
Shanghai Zhihua ChemTech Co., Ltd.

Contact:+86-13774313779

Address:Room 817 Suite B 3333 Shenjiang Road
Chengdu ZY Biochemical Technology Co., LTD

Contact:0086-28-88680086

Address:170 Qingpu Road, Shouan Town, Pujiang County
Jinan Great Chemical Co.,Ltd.

Contact:+86-531-58668191 58668193 58668196 58661173

Address:No 55,Beixiaoxinzhuang West Street,Jinan City, Shandong Province

Relevant to this article

3-Metallierte Enamine; IX. 4-(1-Hydroxyalkylierung) von deprotoniertem 2-(N-Methylanilino)-2-butensaeuremethylester, eine einfache Methode zur Herstellung von Derivaten der 5-Hydroxy-2-oxoalkansaeure-ester

Doi:10.1055/s-1983-30224
(1983)
Convergent synthesis of the FGHI ring system of yessotoxin: Stereoselective construction of the G ring

Doi:10.1016/j.tetlet.2005.04.040
(2005)
Doi:10.1039/jr9550003362
(1955)
Synthesis, spectral characterization and α-chymotrypsin activity of 7-O-substituted derivatives of 7-hydroxy-4-methyl-1-benzopyran-2-one

Doi:10.14233/ajchem.2014.15374
(2014)
Metal-free catalytic olefin hydrogenation: Low-temperature H₂ activation by frustrated lewis pairs

Doi:10.1002/anie.201204007
(2012)
Doi:10.1021/ja01368a049
(1930)

Article Doi

DOI: 10.1021/ja01255a015

Source and publish data: