Scholarly article on Benzene, 1,1',1''-(3-methoxy-1-cyclopropene-1,2,3-triyl)tris- 32141-20-1 from Journal of the American Chemical Society p. 5991,5993

DOI: 10.1021/ja01555a026

Source and publish data:

Journal of the American Chemical Society p. 5991,5993 (1958)

Update date:2022-08-11

Topics:

Authors:

Breslow Breslow

Yuan Yuan

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

Article abstract of DOI:10.1021/ja01555a026

Full text of DOI:10.1021/ja01555a026

Products guided by the article

Product name:Benzene, 1,1',1''-(3-methoxy-1-cyclopropene-1,2,3-triyl)tris-

Cas No:32141-20-1

R&D Labs maybe for 32141-20-1

Laohekou Jinghong Chemical Co.,Ltd

Contact:+86-0710-3702747

Address:163.East，Huagong Road，Laohekou
JiangXi Keyuan Biopharma Co., LTD.

Contact:+86-563-6833666

Address:Guangde Fine Chemical Zone, Anhui Province, China
Suqian Ruixing Chemical Co., Ltd.

Contact:+86-527-80805666（总机）;84836008(销售)

Address:3 Jingsilu, Zone north, Hubin Xincheng Development Park, Suqian, China
Hubei Xinghuo Chemical Co., Ltd.,

Contact:13925817279 13907299441

Address:Xinghuo Fine Chemistry Industrial Park, Xiaochang County, Hubei Province, China
CHENGDU CHENLV HERB CO.,LTD

Contact:+86-28-88523492

Address:714rooms of Time Square, Pujiang County

Relevant to this article

Reactions of ZnR₂ compounds with dibenzoyl: Characterisation of the alkyl-transfer products and a striking product-inhibition effect

Doi:10.1002/chem.201101997
(2011)
SYNTHESIS OF N⁴-ACYLSPERMIDINES

Doi:10.1016/S0040-4039(01)91005-6
(1984)
Synthesis and antimicrobial activity of some novel 2-(p-substituted-phenyl)-5-substituted-carbonylaminobenzoxazoles.

Doi:10.1016/S0014-827X(01)01143-0
(2002)
ROUTES TO FLUOROAROMATICS

Doi:10.1016/S0022-1139(00)83347-3
(1985)
1,1-Difluoro-3-aryl(heteroaryl)-1: H -pyrido[1,2- c] [1,3,5,2]oxadiazaborinin-9-ium-1-uides: Synthesis; Structure; and photophysical, electrochemical, and BSA-binding studies

Doi:10.1039/c7nj04032f
(2018)
Generation of Halomethyl Radicals by Halogen Atom Abstraction and Their Addition Reactions with Alkenes

Doi:10.1021/jacs.9b05921
(2019)

Article Doi

DOI: 10.1021/ja01555a026