1410772-80-3

Basic information

• Product Name: C₁₅H₁₄N₄S
• CAS NO: 1410772-80-3
• Molecular Weight: 282.369
• Mol File: 1410772-80-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₁₅H₁₄N₄S(CAS DataBase Reference)
• NIST Chemistry Reference: C₁₅H₁₄N₄S(1410772-80-3)
• EPA Substance Registry System: C₁₅H₁₄N₄S(1410772-80-3)

Safety Data

• Hazardous Substances Data: 1410772-80-3(Hazardous Substances Data)

Upstream product

• 76423-99-9 dimethyl N-(1,3-benzothiazol-2-yl) dithio imidocarbonate 
• 62-53-3 aniline 
• 1009735-07-2 C₁₅H₁₃N₃S₂ 
• 74-89-5 methylamine 

Relevant articles and documents

A synthetic method to access symmetric and non-symmetric 2-(N,N'-disubstituted)guanidinebenzothiazoles

Symmetric and non-symmetric 2-(N-H, N-methyl, N-ethylenyl and N-aryl)guanidinebenzothiazoles were synthesized from the reaction of ammonia, methylamine, pyrrolidine and aniline with dimethyl benzo[d]thiazol-2-yl- carbonodithioimidate (5) as intermediate. The products were characterized by 1H-, 13C-NMR spectroscopy and three of them by X-ray diffraction analysis. HN-phenyl protons formed intramolecular hydrogen bonds that assist the stereochemistry of the second substituent, whereas the HN-alkyl protons were involved in intermolecular hydrogen bonding.