Scholarly article on 1,2-Dihydro-1-methyl-2,3,1-benzodiazaborine 4885-27-2 from Journal of the American Chemical Society p. 433 - 436

DOI: 10.1021/ja01057a028

Source and publish data:

Journal of the American Chemical Society p. 433 - 436 (1964)

Update date:2022-08-04

Topics:

Authors:

Dewar,M.J.S.

Dougherty,R.C.

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

Article abstract of DOI:10.1021/ja01057a028

Full text of DOI:10.1021/ja01057a028

Products guided by the article

Product name:1,2-Dihydro-1-methyl-2,3,1-benzodiazaborine

Cas No:4885-27-2

R&D Labs maybe for 4885-27-2

Xi'an HO-SHINE Bio-Technology Co., Ltd

Contact:+86 (29) 8248-5435/18292020086

Address:No.6 Shiyuan Road Xian City Shaanxi Province, 710048 China
Anhui Redstar Pharmaceutical Corp., Ltd

Contact:+86-563-5120837

Address:Jingxian Industrial Development Zone, Anhui , China
Shanghai Hanshare Industry Co.,Ltd.

Contact:86 21 20960688

Address:RM902-903,Building E, Wanda Plaza,No.26,Zhoukang Road, Pudong District, Shanghai, China
MS( MAOSHENG )Chemical CO.,LTD

Contact:+86-519-82726678.82726378

Address:TAOXI INDUSTRY ZONE JINTAN
Nanjing Fubang Chemical Co.,Ltd

Contact:+86-25-83179199

Address:5F,Tianzheng international plaza,No399 Zhongyang Road ,Nanjing China

Relevant to this article

Efficient iodine catalyzed three components domino reaction for the synthesis of 1-((phenylthio)(phenyl)methyl)pyrrolidin-2-one derivatives possessing anticancer activities

Doi:10.1039/c2ob25530h
(2012)
Synthesis of new γ-lactones from preactivated monosubstituted pyrazines and TMS-ketene acetals

Doi:10.1139/v2012-016
(2012)
HYDROXYAZOBENZENES: SYNTHESIS AND ANTIMICROBIAL ACTIVITY

Doi:10.1007/BF00767262
(1991)
gem-DINITRO COMPOUNDS IN ORGANIC SYNTHESIS. 1. SYNTHESIS OF FUNCTIONALLY SUBSTITUTED POLYNITRO COMPOUNDS WITH THE USE OF THE UNIVERSAL SYNTHON, ETHYL DINITROACETATE

Doi:10.1007/BF01172267
(1991)
Palladium-Catalyzed Synthesis of Amides and Peptides

Doi:10.1016/0040-4039(91)80241-W
(1991)
Short Synthesis of (+/-)-Bakuchiol via a Geranylindium Reagent

Doi:10.1039/P19910002395
(1991)

Article Doi

DOI: 10.1021/ja01057a028