5 Styryl 2 benzimidazolylurethanes as potential anthelminthics

DOI: 10.1135/cccc19751089

Source and publish data:

Collection of Czechoslovak Chemical Communications p. 1089 - 1094 (1975)

Update date:2022-08-04

Topics:

Authors:

Budesinsky

Sluka Sluka

Novak Novak

Danek Danek

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

Article abstract of DOI:10.1135/cccc19751089

Full text of DOI:10.1135/cccc19751089

Products guided by the article

Product name:[5-(4-methoxy-styryl)-1⁽³⁾H-benzoimidazol-2-yl]-carbamic acid methyl ester

Cas No:56495-07-9

R&D Labs maybe for 56495-07-9

Changzhou Foreign Trade Corp

Contact:+86-519-86623222

Address:29F/D, 99 Yanling West Road, Changzhou, Jiangsu, China
Xi'an Costrong Pharmaceutical Co., Ltd.

Contact:029- 68576496

Address:Room 2004,Shuibao Building,No.190,South Erhuan Rd, Yanta District,Xi'an,Shaan Xi,China
WUHAN WELLSONG INT'L CO.,LTD

Contact:+86-27-85733560

Address:NO.308,QINGNIAN RD.,WUHAN,CHINA
Huaihua Baohua Biotechnology Co.,Ltd

website:http://www.baochengchem.com

Contact:86-519-82698291

Address:HouYang chemical development zone,Jintan,Jiangsu,China (213200)
Changzhou Litong Chemical Co., Ltd.

website:http://www.litonchem.com/

Contact:+86-519-86301238

Address:Laoba Rd, Hutang town Changzhou Jiangsu

Relevant to this article

Efficient Control of the Stereoselectivity in Reactions of 2-Oxy-Substituted Benzylic Radicals

Doi:10.1002/hlca.19950780422
(1995)
Synthesis of a C₁-C₁₄ subunit of the macrodiolide antibiotics pamamycin-607 and pamamycin-635B

Doi:10.1016/0040-4039(95)00471-N
(1995)
Doi:10.1021/je60021a038
(1964)
Highly diastereodivergent synthesis of tetrasubstituted cyclohexanes catalyzed by modularly designed organocatalysts

Doi:10.1002/anie.201404072
(2014)
Palladium-catalyzed alkoxycarbonylation of conjugated dienes under acid-free conditions: Atom-economic synthesis of β,γ-unsaturated esters

Doi:10.1002/anie.201404563
(2014)
A simple method for α-position deuterated carbonyl compounds with pyrrolidine as catalyst

Doi:10.1002/jlcr.3210
(2014)

Article Doi