SYNTHESIS AND STRUCTURE OF NITRO DERIVATIVES OF PENTANE. COMMUNICATION 2. 1,1,1,3,5,5,5-HEPTANITROPENTANE AND ITS 3-FLUORO AND 3-CHLORO DERIVATIVES

DOI: 10.1007/BF00995687

Source and publish data:

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science p. 504 - 510 (1984)

Update date:2022-08-12

Topics:

Authors:

Atovmyan, L. O.

Golovina, N. I.

Eremenko, L. T.

Zhitomirskaya, N. G.

Oreshko, G. V.

Fadeev, M. A.

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

Article abstract of DOI:10.1007/BF00995687

Full text of DOI:10.1007/BF00995687

Products guided by the article

Product name:1,1,1,3,5,5,5-Heptanitro-pentane

Cas No:20919-99-7

R&D Labs maybe for 20919-99-7

Shenyang NovPharm Technology Co., Ltd.

Contact:.+86-24-24165786

Address:Room 306, Hongjin Mansion, No. 36-1, Wanliutang Rd., Shenhe District, Shenyang, Liaoning, P.R.C.
Chameleon Specialty Chemicals

Contact:+44 7958 511245

Address:PO Box 469, Manchester, UK
Shanghai Egoal Chemical Co.,Ltd

Contact:+86-21-50333091

Address:Yangming Garden Square 3,YangGao North Road 1188, Pudong New District, Shanghai
Dongguan Albiya Energy Science and Technology Co.,Ltd

Contact:+86-769-22181286

Address:Huanan Industial Park, Dongguan,China
Taixing Shenfeng Chemical Co., Ltd.

Contact:+86-523-87117033, 87117666

Address:4# Yinsanlu, Huangqiao town, Taixing, Jiangsu, China.

Relevant to this article

New microwave dielectric ceramics BaLn₂(MoO₄) ₄ (Ln = Nd and Sm) with low loss

Doi:10.1111/j.1551-2916.2011.04727.x
(2011)
Molecular oxygen-assisted oxidative dehydrogenation of ethylbenzene to styrene with nanocrystalline Ti_1-xV_xO₂

Doi:10.1039/c1gc15907k
(2012)
Efficient regio- and stereoselective conversions of oxiranes and aziridines into β-(nitrooxy)-substituted alcohols and amines by using bismuth nitrate

Doi:10.1002/hlca.200790002
(2007)
Doi:10.1021/jo01075a034
(1960)
A facile heterogeneous system for persulfate activation by CuFe2O4 under LED light irradiation

Doi:10.1039/c9ra05574f
(2019)
Hydrolysis of glycosylpyridinium ions by anomeric-configuration-inverting glycosidases

Doi:10.1016/0008-6215(93)84156-Z
(1993)

Article Doi