Thiocarbamoylation of amine-containing compounds 3. 5-(N′,N′-dimethylthioureido)salicylic acid. Synthesis and reactions

DOI: 10.1007/BF02498274

Source and publish data:

Russian Chemical Bulletin p. 2290 - 2293 (1999)

Update date:2022-08-04

Topics:

Authors:

Van Boi, Luu

Al-Ebaisat

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

Article abstract of DOI:10.1007/BF02498274

Thiocarbamoylation of 5-aminosalicylic acid with tetramethylthiuram disulfide afforded 5-(N′,N′-dimethylthioureido)salicylic acid. Treatment of the latter with mineral acids or Ac₂O gave 5-isothiocyanatosalicylic acid, whose reaction with ethan

Full text of DOI:10.1007/BF02498274

Products guided by the article

Product name:5-(N',N'-dimethylthioureido)salicylic acid

Cas No:264257-12-7

R&D Labs maybe for 264257-12-7

Yangzhou Siyu Chemical Co.,Ltd.

Contact:+86-514-87325867 13358126196

Address:Room 620 Exposition Pavilion，No. 98 Huaihai Road,Guangling District，Yangzhou City, Jiangsu Province
Chengdu ZY Biochemical Technology Co., LTD

Contact:0086-28-88680086

Address:170 Qingpu Road, Shouan Town, Pujiang County
Exploiter Molybdenum Co.,Ltd

Contact:86-379-63338609

Address:Jiudian Village,Deting Town,Song County,Luoyang
Disynthesis Chemical Technology Co. Ltd.

Contact:+86-571-88194596

Address:Dengyun road 380, Gongshu district, Hangzhou city, China
Tai zhou world Pharm & Chem Co., Ltd

Contact:+86-576-85301198

Address:Rome 1001,wangjiang plaza,unti 2,jinshan east Road linhai,zhejiang,china

Relevant to this article

Observations concerning the existence and reactivity of free α-amino aldehydes as chemical intermediates: Evidence for epimerization-free adduct formation with various nucleophiles [11]

Doi:10.1021/ja000136x
(2000)
Effective approach to ureas through organocatalyzed one-pot process

Doi:10.1016/j.tetlet.2017.11.030
(2018)
Na⁺/K⁺-ATPase-Targeted Cytotoxicity of (+)-Digoxin and Several Semisynthetic Derivatives

Doi:10.1021/acs.jnatprod.9b01060
(2020)
Synthesis of (23R)- and (23S)-23H-isocalysterols, marine sterols with a cyclopropene moiety in the side chain

Doi:10.1002/(sici)1099-0690(200003)2000:6<1027::aid-ejoc1027>3.0.co;2-e
(2000)
A survey of cyclic replacements for the central diamide moiety of inhibitors of inosine monophosphate dehydrogenase

Doi:10.1016/S0960-894X(02)00641-8
(2002)
Doi:10.1039/jr9410000566
(1941)

Article Doi