2741-08-4

Basic information

• Product Name: Thiourea, N-ethyl-N'-(phenylmethyl)-
• Synonyms: 1-ethyl-3-benzyl thiourea;N-Aethyl-N'-benzyl-thioharnstoff;N-ethyl-N'-benzyl-thiourea;N-Benzyl-N'-ethyl-thioharnstoff;Thiourea,N-ethyl-N'-(phenylmethyl);(ethylamino)[benzylamino]methane-1-thione;1-Ethyl-3-benzyl-thioharnstoff
• CAS NO: 2741-08-4
• Molecular Formula: C10H14N2S
• Molecular Weight: 194.29700
• Mol File: 2741-08-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Thiourea, N-ethyl-N'-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Thiourea, N-ethyl-N'-(phenylmethyl)-(2741-08-4)
• EPA Substance Registry System: Thiourea, N-ethyl-N'-(phenylmethyl)-(2741-08-4)

Safety Data

• Hazardous Substances Data: 2741-08-4(Hazardous Substances Data)

Upstream product

• 542-85-8 Ethyl isothiocyanate 
• 100-46-9 benzylamine 
• 856768-18-8 Ethyl-thiocarbamic acid O-(4-chloro-phenyl) ester 
• 2438-91-7 μ-disulfido-1,2-dithio-dicarbonic acid bis-ethylamide 

Downstream Products

• 1096570-91-0 3-ethyl-2-(N-benzylimino)-5-methyl-4-phenyl-1,3-thiazoline 
• 76070-79-6 C₁₁H₁₆N₄S*2ClH 
• 76070-68-3 3-amino-4-benzyl-5-ethylimino-4,5-dihydro-1,2,4-thiadiazole 
• 63796-18-9 1-Benzyl-3-ethyl-carbodiimid 

Relevant articles and documents

A convenient one-pot three component approach to synthesis of highly substituted iminothiazolines

An efficient one-pot three component method was developed for the synthesis of highly substituted 2-iminothizolines by the reaction of isothiocyanates, primary amines and α-bromoketones in ambient temperature. The reaction produced the desired products in a completely regioselective manner in excellent yields (78-94%). The Japan Institute of Heterocyclic Chemistry.

Biocidal isothiourea compounds

Novel biocidal S-aminoalkyl isothiourea compounds have the general structural formula STR1 wherein X is halogen; R is a straight or branched chain alkyl radical containing 5 to 20 carbon atoms; R1 is selected from the group consisting of alkyl