213993-31-8

Basic information

• Product Name: Cyclohexanemethanol, 2-amino-, (1S,2S)- (9CI)
• Synonyms: Cyclohexanemethanol, 2-amino-, (1S,2S)- (9CI);(1S,2S)-2-aMino-cyclohexylMethanol
• CAS NO: 213993-31-8
• Molecular Formula: C₇H₁₅NO
• Molecular Weight: 129.2001
• Product Categories: AMINEPRIMARY
• Mol File: 213993-31-8.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 218.8±13.0 °C(Predicted)
• Appearance: /
• Density: 0.974±0.06 g/cm3(Predicted)
• PKA: 15.05±0.10(Predicted)
• CAS DataBase Reference: Cyclohexanemethanol, 2-amino-, (1S,2S)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanemethanol, 2-amino-, (1S,2S)- (9CI)(213993-31-8)
• EPA Substance Registry System: Cyclohexanemethanol, 2-amino-, (1S,2S)- (9CI)(213993-31-8)

Safety Data

• Hazardous Substances Data: 213993-31-8(Hazardous Substances Data)

Upstream product

• 24716-94-7 (1S,2S)-2-aminocyclohexanecarboxylic acid ethyl ester 
• 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 
• 191986-95-5 (1S,2S)-ethyl 2-((S)-1-phenylethylamino)cyclohexanecarboxylate 
• 191986-93-3 (1R,2S)-ethyl 2-((S)-1-phenylethylamino)cyclohexanecarboxylate 
• 1346773-51-0 (1R,2S)-ethyl 2-((S)-1-phenylethylamino)cyclohexanecarboxylate hydrochloride 
• 1346773-51-0 (1S,2S)-ethyl 2-((S)-1-phenylethylamino)cyclohexanecarboxylate hydrochloride 
• 1260890-62-7 (1S,2S)-2-[(S)-1-phenylethylamino]cyclohexylmethanol 
• 53898-03-6 2-(S-1-phenylethylamino)-cyclohex-1-enecarboxylic acid ethyl ester 
• 1655-07-8 ethyl 2-oxocyclohexane carboxylate 

Downstream Products

• 1379691-06-1 (1S,2S)-2-(benzothiazol-2-ylamino)cyclohexylmethanol 
• 144478-68-2 (2R,3aR,7aS)-1-Benzoyl-octahydro-indole-2-carbonitrile 
• 144478-69-3 (2S,3aR,7aS)-1-Benzoyl-octahydro-indole-2-carbonitrile 
• 144540-73-8 Methanesulfonic acid (1S,2S)-2-(benzoyl-cyanomethyl-amino)-cyclohexylmethyl ester 
• 1158650-42-0 N-Cyanomethyl-N-((1S,2S)-2-hydroxymethyl-cyclohexyl)-benzamide 
• 144478-67-1 ((1S,2S)-2-Hydroxymethyl-cyclohexylamino)-acetonitrile 
• 956325-23-8 tert-butyl ((1S,2S)-2-(hydroxymethyl)cyclohexyl)carbamate 

Relevant articles and documents

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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

Novel Compounds

Compounds of Formulae I, or pharmaceutically acceptable salts thereof: wherein X, R1, R2 and R3 are as defined in the specification as well as salts and pharmaceutical compositions including the compounds are prepared. They are useful in therapy, in particular in the management of pain.