1379691-06-1

Basic information

• Product Name: (1S,2S)-2-(benzothiazol-2-ylamino)cyclohexylmethanol
• CAS NO: 1379691-06-1
• Molecular Weight: 262.376
• Mol File: 1379691-06-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1S,2S)-2-(benzothiazol-2-ylamino)cyclohexylmethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2S)-2-(benzothiazol-2-ylamino)cyclohexylmethanol(1379691-06-1)
• EPA Substance Registry System: (1S,2S)-2-(benzothiazol-2-ylamino)cyclohexylmethanol(1379691-06-1)

Safety Data

• Hazardous Substances Data: 1379691-06-1(Hazardous Substances Data)

Upstream product

• 5691-19-0 rac-trans-2-aminocyclohexanecarboxylic acid 
• 1655-06-7 (1R,2S)-ethyl 2-hydroxycyclohexanecarboxylate 
• 1379691-07-2 (1S,2S)-2-(N-benzyl-N-((S)-α-methylbenzyl)amino)cyclohexanecarboxylic acid 
• 1379691-05-0 (1R,2S)-ethyl 2-(N-benzyl-N-((S)-α-methylbenzyl)amino)cyclohexanecarboxylate 
• 1617-22-7 cyclohex-1-enecarboxylic acid ethyl ester 
• 1315564-11-4 ethyl 2-(4-methylbenzenesulfonyloxy)cyclohexanecarboxylate 
• 615-20-3 2-chlorobenzo[d][1,3]thiazole 
• 213993-31-8 (1S,2S)-2-amino-cyclohexylmethanol 

Relevant articles and documents

Isothiourea-mediated asymmetric O- to C-carboxyl transfer of oxazolyl carbonates: Structure-selectivity profiles and mechanistic studies

The structural motif within a series of tetrahydropyrimidine-based isothioureas necessary for generating high asymmetric induction in the asymmetric Steglich rearrangement of oxazolyl carbonates is fully explored, with crossover and dynamic 19F NMR experiments used to develop a mechanistic understanding of this transformation. Copyright