Scholarly article on 4-allyloxy-benzaldehyde-selenosemicarbazone 119658-67-2 from Bulletin des Societes Chimiques Belges p. 684,689,690

DOI: 10.1111/j.1540-8191.2001.tb00551.x

Source and publish data:

Bulletin des Societes Chimiques Belges p. 684,689,690 (1956)

Update date:2022-07-29

Topics:

Authors:

Huls Huls

Renson Renson

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

Article abstract of DOI:10.1111/j.1540-8191.2001.tb00551.x

Full text of DOI:10.1111/j.1540-8191.2001.tb00551.x

Products guided by the article

Product name:4-allyloxy-benzaldehyde-selenosemicarbazone

Cas No:119658-67-2

R&D Labs maybe for 119658-67-2

CGeneTech (Suzhou, China) Co., Ltd.

Contact:+86-512-62956962

Address:Room 101，Bld C11,218 Xinghu Rd.,Suzhou industrial Park
Xian Lyphar Biotech Co., Ltd.

Contact:0086-29-89196322

Address:North of the Fifth Keji Road, Hi-Tech Industrial Zone, Xi'an City, Shaanxi Province, China
Zhangjiagang Jianing Import & Export Co.,Ltd.

Contact:086-512-55379012 13913607595

Address:NO.1 Guotai North Road Zhangjiagang Economic Development Zone,215600,Jiangsu,China
Beijing ZhongDaXinHe Chemical Product Co.,Ltd(expird)

Contact:010-52876516

Address:tongzhoubeiyuan
Beijing Mashi Fine Chemical Co.,Ltd.

Contact:+86-10-61271592

Address:Room 506, Section B, Kaichi Mansion, Industrial Development

Relevant to this article

New rhenium(III) complexes with fluorinated β-diketones

Doi:10.1134/S1070328412030037
(2012)
Diversity-oriented derivatization of BODIPY based on regioselective bromination

Doi:10.1039/c2ob07004a
(2012)
Alternative mild route to the synthesis of 4-methylenecyclohex-2-enone, a key moiety of the anticancer compounds ottelione A and B

Doi:10.1080/00397911.2011.607936
(2012)
Renin Inhibitory Peptides. A β-Aspartyl Residue as a Replacement for the Histidyl Residue at the P-2 Site

Doi:10.1021/jm00167a009
(1990)
Synthesis, reactivity, and computational analysis of halophosphines supported by dianionic guanidinate ligands

Doi:10.1021/ja300587z
(2012)
Dinickel(ii) complexes: Preparation and catalytic activity

Doi:10.1039/c2dt11398h
(2012)

Article Doi

DOI: 10.1111/j.1540-8191.2001.tb00551.x