158414-45-0

Basic information

• Product Name: (1S,2R)-(+)-2-AMINOCYCLOHEXANECARBOXYLIC ACID HYDROCHLORIDE
• Synonyms: (1S,2R)-CIS-2-AMINO-1-CYCLOHEXANE-CARBOXYLIC ACID HYDROCHLORIDE;(1S,2R)-(+)-2-AMINOCYCLOHEXANECARBOXYLIC ACID HYDROCHLORIDE;(1S,2R)-(+)-2-Aminocyclohexanecarboxylic acidhydrochloride,97%
• CAS NO: 158414-45-0
• Molecular Formula: C7H14ClNO2
• Molecular Weight: 179.64
• Mol File: 158414-45-0.mol
• Article Data: 4

Chemical Properties

• Melting Point: 233-236 °C
• Boiling Point: 280°Cat760mmHg
• Flash Point: 123.1°C
• Appearance: /
• Density: 1.133g/cm³
• Vapor Pressure: 0.00103mmHg at 25°C
• Refractive Index: 1.503
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: (1S,2R)-(+)-2-AMINOCYCLOHEXANECARBOXYLIC ACID HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,2R)-(+)-2-AMINOCYCLOHEXANECARBOXYLIC ACID HYDROCHLORIDE(158414-45-0)
• EPA Substance Registry System: (1S,2R)-(+)-2-AMINOCYCLOHEXANECARBOXYLIC ACID HYDROCHLORIDE(158414-45-0)

Safety Data

• Hazard Codes: C
• Statements: 34
• Safety Statements: 45-36/37/39-26
• Hazardous Substances Data: 158414-45-0(Hazardous Substances Data)

Usage

Chemical Properties

Beige crystalline powder

InChI:InChI=1/C7H13NO2/c8-6-4-2-1-3-5(6)7(9)10/h5-6H,1-4,8H2,(H,9,10)/t5-,6+/m0/s1

Upstream product

• 874292-57-6 (1R,6S)-7-azabicyclo[4.2.0]octan-8-one 
• 1436-60-8 ethyl cis-2-amino-1-cyclohexanecarboxylate 
• 34314-73-3 C₁₁H₁₉NO₃Si 
• 110-83-8 cyclohexene 
• 24716-92-5 (±)-cis-2-aminocyclohexane-1-carboxylic acid hydrochloride 
• 209128-50-7 (±)-cis-N-tert-butyloxycarbonyl-2-aminocyclohexanecarboxylic acid 
• 1436-60-8 ethyl trans-2-amino-1-cyclohexanecarboxylate 
• 34314-73-3 C₁₁H₁₉NO₃Si 

Downstream Products

• 24716-92-5 (±)-trans-2-aminocyclohexanecarboxylic acid hydrochloride 
• 1214740-68-7 C₇H₈O₃S*C₁₄H₁₉NO₂ 

Relevant articles and documents

Solid-phase synthesis of 6,7-cycloalkane-fused 1,4-diazepane-2,5-diones via a cyclization/release strategy

A solid-phase synthesis procedure for the parallel preparation of 6,7-cycloalkane-fused 1,4-diazepane-2,5-diones is described. The methodology applies α- and alicyclic β-amino acid building blocks to construct the seven-membered heterocyclic core, while a

The first direct enzymatic hydrolysis of alicyclic β-amino esters: A route to enantiopure cis and trans β-amino acids

The first direct enzymatic method is reported for the synthesis of cis and trans βamino acid enantiomers through the lipase-catalyzed enantioselective hydrolysis of alicyclic β esters in organic media. High enantioselectivities (E usually > 001) were observed when the Candida antarctica lipase B catalyzed reactions were performed with H2O (0.5 equivalents) in iP iPr2O at 5°C. The resolved products, obtained in good yields (≥42%), could be easily separated.