116261-09-7

Basic information

• Product Name: Cyclohexanecarboxamide, 2-(hydroxymethyl)-, cis- (9CI)
• Synonyms: Cyclohexanecarboxamide, 2-(hydroxymethyl)-, cis- (9CI)
• CAS NO: 116261-09-7
• Molecular Formula: C8H15NO2
• Molecular Weight: 157.2102
• Product Categories: AMIDE
• Mol File: 116261-09-7.mol

Chemical Properties

• Boiling Point: 357.4±11.0 °C(Predicted)
• Appearance: /
• Density: 1.095±0.06 g/cm3(Predicted)
• PKA: 15.05±0.10(Predicted)
• CAS DataBase Reference: Cyclohexanecarboxamide, 2-(hydroxymethyl)-, cis- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanecarboxamide, 2-(hydroxymethyl)-, cis- (9CI)(116261-09-7)
• EPA Substance Registry System: Cyclohexanecarboxamide, 2-(hydroxymethyl)-, cis- (9CI)(116261-09-7)

Safety Data

• Hazardous Substances Data: 116261-09-7(Hazardous Substances Data)

Upstream product

• 144540-72-7 trans-hexahydrophthalide 
• 4336-20-3 dimethyl 1,2-cyclohexanedicarboxylate 
• 88335-91-5 cyclohexane-1,2-dicarboxylic acid monomethyl ester 
• 89395-29-9 (3aR,7aS)-hexahydroisobenzofuran-1-one 
• 116174-39-1 ((1S,2S)-2-Hydroxymethyl-cyclohexyl)-pyrrolidin-1-yl-methanone 
• 65376-02-5 (1S,6R)-8-oxabicyclo[4.3.0]nonan-7-one 

Downstream Products

• 213993-31-8 (1S,2S)-2-amino-cyclohexylmethanol 
• 144478-67-1 ((1S,2S)-2-Hydroxymethyl-cyclohexylamino)-acetonitrile 

Relevant articles and documents

Precursors for the production of chiral 1,3-aminoalcohols

The disclosure describes novel precursors for the preparation of chiral 1,3-aminoalcohols. The precursors are chiral 4-hydroxycarboxamides, 4-hydroxyhydroxamic acids, or 4-hydroxyhydrazides produced from chiral gamma-lactones, which in turn are derived from 1,4-diols by stereoselective oxidation. The chiral 4-hydroxycarboxamides, 4-hydroxyhydroxamic acids, or 4-hydroxyhydrazides are converted into chiral 1,3-aminoalcohols by stereospecific rearrangement.

Stereoselective synthesis of a trans-octahydroindole derivative, precursor of trandolapril (RU 44 570), an inhibitor of angiotensin converting enzyme

We describe a stereoselective synthesis of the trans-octahydroindole-2-carboxylic acid 2 a key intermediate in the elaboration of Trandolapril (RU 44 570) 1. The optically active starting material used was obtained by an enzymatic hydrolysis.