Scholarly article on 5-(4-chloro-phenoxy)-benzo[a]phenazine 102442-74-0 from Journal of the American Chemical Society p. 6057,6059

DOI: 10.1021/ja01555a041

Source and publish data:

Journal of the American Chemical Society p. 6057,6059 (1958)

Update date:2022-08-05

Topics:

Authors:

Awad Awad

Hafez Hafez

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

Article abstract of DOI:10.1021/ja01555a041

Full text of DOI:10.1021/ja01555a041

Products guided by the article

Product name:5-(4-chloro-phenoxy)-benzo[a]phenazine

Cas No:102442-74-0

R&D Labs maybe for 102442-74-0

Joyochem Co., Ltd.

website:https://sdjingyuan.lookchem.com/

Contact:86-531-82687998

Address:Factory Building 11, Jinan Comprehensive free trade zone, Shandong, China
shijiazhuang shuanglian chemical industry co.,ltd

Contact:0311-82190302

Address:Luquan Intersection , Shijiazhuang--Taiyuan Expressway，Shijiazhuang City
HANGZHOU ZHONGCHANG SCIENTIFIC CO.,LTD

Contact:+86-571-88932183

Address:Hangzhou
Wuxi Olite Chemical Co., Ltd.

Contact:86-510-82853889

Address:Rm.3732, No.18-2,Yonghe Rd.,Wuxi,Jiangsu,214023,China
Zhejiang Tianyu Pharmaceutical Co., Ltd.

Contact:+86-576-84177669, 89189665,89189688,84168770

Address:Jiangkou Development Zone, Huangyan, Taizhou City, Zhejiang

Relevant to this article

β-CARBONYL RADICALS AS THREE-CARBON BUILDING BLOCKS FOR CARBON-CARBON BOND FORMING REACTIONS

Doi:10.1016/S0040-4020(01)97181-9
(1985)
Phenylethynyl-pyrrolo[1,2-a]pyrazine: A new potent and selective tool in the mGluR5 antagonists arena

Doi:10.1016/j.bmcl.2008.02.024
(2008)
LDA-mediated selective addition reaction of vinylidenecyclopropanes with aldehydes, ketones, and enones: Facile synthesis of vinylcyclopropenes allenols, and 1,3-enynes

Doi:10.1021/ol800463k
(2008)
Potent, nonpeptide inhibitors of human mast cell tryptase. Synthesis and biological evaluation of novel spirocyclic piperidine amide derivatives

Doi:10.1016/j.bmcl.2008.01.093
(2008)
Bioactive products from singlet oxygen photooxygenation of cannabinoids

Doi:10.1016/j.ejmech.2017.11.043
(2018)
A new synthesis of temozolomide

Doi:10.1039/b205614c
(2002)

Article Doi

DOI: 10.1021/ja01555a041