Scholarly article on 1,1-Dimethyl-2,2-bis-trifluoromethyl-diarsane 19863-21-9 from Journal of Inorganic and Nuclear Chemistry p. 35

DOI: 10.1016/0022-1902(74)80653-6

Source and publish data:

Journal of Inorganic and Nuclear Chemistry p. 35 (1974)

Update date:2022-08-05

Topics:

Authors:

Byrne Byrne

Russ Russ

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

Article abstract of DOI:10.1016/0022-1902(74)80653-6

Full text of DOI:10.1016/0022-1902(74)80653-6

Products guided by the article

Product name:1,1-Dimethyl-2,2-bis-trifluoromethyl-diarsane

Cas No:19863-21-9

R&D Labs maybe for 19863-21-9

Jitat Company Ltd

Contact:852-27701081

Address:Room 2509, New Tech Plaza, 34 Tai Yau St., San Po Kong, HK
SPRING CHEMICAL INDUSTRY CO.,LTD

Contact:86-187-66672125

Address:linchi industry park.zouping
Huayang chemical Co., LTD

Contact:+86-18653358619

Address:zibo
Suzhou Tianma Specialty Chemicals Co.,Ltd

Contact:+86-512-68090577

Address:#199, Huayuan Rd, Mudu, Suzhou, Jiangsu, CHINA
Shenzhen Feiming Science and Technology Co,. Ltd

Contact:+86-755-85232577

Address:#B2309, Fenglin International Center ,Jixiang Road, Longcheng street, LongGang District, Shenzhen city, Guangdong province, China.

Relevant to this article

Components of laser trilobum

Doi:10.1007/s10600-010-9592-7
(2010)
Doi:10.1021/ja01263a013
(1942)
Discovery and preliminary SAR studies of a novel, nonsteroidal progesterone receptor antagonist pharmacophore

Doi:10.1021/jm9801915
(1998)
Nucleosides and nucleotides. Part 212: Practical large-scale synthesis of 1-(3-C-ethynyl-β-D-ribo-pentofuranosyl)cytosine (ECyd), a potent antitumor nucleoside. Isobutyryloxy group as an efficient anomeric leaving group in the Vorbrüggen glycosylation reaction

Doi:10.1016/S0040-4020(01)01249-2
(2002)
D₂-symmetric chiroporphyrins derived from (1R)-cis-hemicaronaldehydic acid: Preparation and spectral characterization

Doi:10.1002/(sici)1099-0690(200002)2000:4<583::aid-ejoc583>3.0.co;2-e
(2000)
A new approach to peptide synthesis

Doi:10.1039/a706658i
(1997)

Article Doi

DOI: 10.1016/0022-1902(74)80653-6