62302-16-3

Basic information

• Product Name: 1,2,4-Thiadiazol-5(2H)-imine, 2,3-diphenyl-, monohydrochloride
• CAS NO: 62302-16-3
• Molecular Formula: C14H11N3S.ClH
• Molecular Weight: 289.788
• Mol File: 62302-16-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,2,4-Thiadiazol-5(2H)-imine, 2,3-diphenyl-, monohydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,4-Thiadiazol-5(2H)-imine, 2,3-diphenyl-, monohydrochloride(62302-16-3)
• EPA Substance Registry System: 1,2,4-Thiadiazol-5(2H)-imine, 2,3-diphenyl-, monohydrochloride(62302-16-3)

Safety Data

• Hazardous Substances Data: 62302-16-3(Hazardous Substances Data)

Upstream product

• 6630-99-5 1,2,3,4-thiatriazole-5-amine 
• 38430-05-6 (E)-N-phenylbenzimidoyl chloride 

Downstream Products

• 62302-12-9 2,3,5,6-tetraphenyl-3,5-dihydro-4λ⁴-[1,2,4]thiadiazolo[5,1-e][1,2,4]thiadiazole 
• 80884-71-5 2,3-diphenyl-5-ethylcarbamoylimino-δ³-1,2,4-thiadiazoline 
• 80884-76-0 N¹-(4,4-dioxo-δ²-1,4,3-dithiazolin-2-yl)-N²-phenylbenzylamidine 
• 80884-63-5 5-benzoylimino-2,3-diphenyl-δ³-1,2,4-thiadiazoline 
• 123180-00-7 2,3-diphenyl-2H-[1,2,4]thiadiazol-5-ylideneamine 
• 55434-77-0 N'-cyano-N-phenylbenzenecarboximidamide 
• 62302-15-2 2-anilino-5,6-diphenyl-5H-4λ⁴-[1,2,4]thiadiazolo[1,5-b][1,2,4]dithiazole 
• 75787-13-2 2,3-diphenyl-5-tosylimino-δ³-1,2,4-thiadiazoline 

Relevant articles and documents

SYNTHESIS OF SYMMETRICAL 1,6-DIHETERO-6aλ4-THIA-3,4-DIAZAPENTALENES FROM 5-AMINO-1,2,3,4-THIATRIAZOLE

1,6-Dioxa-6aλ4-thia-3,4-diazapentalenes 7 and 1,3,4,6-tetraaza-6aλ4-thiapentalenes 15, two new classes of compounds with single bond - no bond resonance, have been prepared by reaction of 5-amino-1,2,3,4-thiatriazole 4 with acyl chlorides and imidoyl chlorides.In the latter case, the salts of 5-imino-Δ3-1,2,4-thiadiazolines 12 were first isolated and subsequently reacted with a second equivalent of imidoyl chloride.This also led to the synthesis of unsimmetrically substituted 1,3,4,6-tetraaza-6aλ4-thiapentalenes.In the presence of bases, the salts 12 decompose via the isolable free bases 13 into N-cyanoamidines 14 and sulfur.Treatment of the dioxathiapentalenes 7 with P4S10, or direct thiobenzoylation of 4 gave the 3,4-diaza-1,6aλ4-trithiapentalenes 9.