Scholarly article on 2-bromo-1,3,4,5-tetramethylbenzene 3349-15-3 from Journal of the American Chemical Society p. 2084,2085

DOI: 10.1021/ja01276a020

Source and publish data:

Journal of the American Chemical Society p. 2084,2085 (1938)

Update date:2022-08-04

Topics:

Authors:

James James

Snell Snell

Weissberger

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

Article abstract of DOI:10.1021/ja01276a020

Full text of DOI:10.1021/ja01276a020

Products guided by the article

Product name:2-bromo-1,3,4,5-tetramethylbenzene

Cas No:3349-15-3

R&D Labs maybe for 3349-15-3

Hangzhou utanpharma Co., Ltd

Contact:86-571-87758773

Address:Room604 ,6F, Block A1-3 Xixi Plaza,No. 588 Wenyi West RD, Hangzhou,310012, China
Buffett (China) Holding Co.,Ltd

Contact:4006570891

Address:
WUHAN WELLSONG INT'L CO.,LTD

Contact:+86-27-85733560

Address:NO.308,QINGNIAN RD.,WUHAN,CHINA
waho int'l company

Contact:+86-579-85206992

Address:No 451 chouzhou north road ,room 1106 int'l business center , yiwu ,china
Tangshan Moneide Trading Co., Ltd.

Contact:+86-315-8309571

Address:2-7-420 Jidong Building Materials Commercial Center, Tangshan, Hebei, 064000 China

Relevant to this article

Acceleration of alkenyltrimethylsilane fluorination under mild conditions using ultrasound

Doi:10.1016/j.ultsonch.2010.02.007
(2010)
Enantioselective epoxidation of β,β-disubstituted enamides with a manganese catalyst and aqueous hydrogen peroxide

Doi:10.1021/acs.orglett.9b00729
(2019)
Doi:10.1021/jm01236a015
(1962)
Doi:10.1039/j39710002637
(1971)
Visible-Light-Promoted Formation of C—C and C—P Bonds Derived from Evolution of Bromoalkynes under Additive-Free Conditions: Synthesis of 1,1-Dibromo-1-en-3-ynes and Alkynylphosphine Oxides

Doi:10.1002/cjoc.202000546
(2021)
A toolbox approach for the rapid evaluation of multi-step enzymatic syntheses comprising a 'mix and match' E. coli expression system with microscale experimentation

Doi:10.3109/10242422.2011.609589
(2011)

Article Doi

DOI: 10.1021/ja01276a020