217799-18-3

Basic information

• Product Name: Cyclohexanecarboxylic acid, 2-amino-, methyl ester, (1S,2S)- (9CI)
• Synonyms: Cyclohexanecarboxylic acid, 2-amino-, methyl ester, (1S,2S)- (9CI);Methyl (1S,2S)-2-aMinocyclohexane-1-carboxylate;METHYL (1S,2S)-2-AMINOCYCLOHEXANE-1-CARBOXYLATE HYDROCHLORIDE
• CAS NO: 217799-18-3
• Molecular Formula: C₈H₁₅NO₂
• Molecular Weight: 157.2102
• Product Categories: CARBOXYLICESTER
• Mol File: 217799-18-3.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Cyclohexanecarboxylic acid, 2-amino-, methyl ester, (1S,2S)- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanecarboxylic acid, 2-amino-, methyl ester, (1S,2S)- (9CI)(217799-18-3)
• EPA Substance Registry System: Cyclohexanecarboxylic acid, 2-amino-, methyl ester, (1S,2S)- (9CI)(217799-18-3)

Safety Data

• Hazardous Substances Data: 217799-18-3(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
Cyclohexanecarboxylic acid, 2-amino-, methyl ester, (1S,2S)(9CI) is used as a chiral compound in the pharmaceutical industry for its potential applications in the development of new drugs or therapeutic agents. Its unique spatial arrangement of atoms and potential biological activity make it a valuable candidate for further research and exploration.
Used in Medicinal Applications:
In the field of medicine, Cyclohexanecarboxylic acid, 2-amino-, methyl ester, (1S,2S)(9CI) is utilized for its potential to contribute to the discovery and creation of novel therapeutic agents. Its chiral nature and possible biological properties could lead to advancements in treating various medical conditions, pending further investigation and validation.

Upstream product

• 932743-49-2 6-benzylamino-cyclohex-1-enecarboxylic acid methyl ester 
• 1062573-96-9 (1S,2S)-2-(4-methoxy-phenylamino)cyclohexane-1-carboxylic acid methyl ester 
• 225779-46-4 6-methoxycarbonyloxycyclohex-1-enecarboxylic acid methyl ester 
• 865780-25-2 methyl 6-hydroxy-cyclohex-1-enecarboxylate 

Downstream Products

• 932743-70-9 (1S,2S)-2-benzyloxycarbonylaminocyclohexane-1-carboxylic acid methyl ester 

Relevant articles and documents

Pd-catalyzed asymmetric allylic aminations with aromatic amine nucleophiles using chiral diaminophosphine oxides: DIAPHOXs

Asymmetric allylic aminations with aromatic amine nucleophiles using Pd-DIAPHOX catalyst systems are described. The asymmetric allylic aminations of various allylic carbonates proceeded using 2-5 mol % of the catalyst and BSA, providing the corresponding

Pd-catalyzed asymmetric allylic amination of Morita-Baylis-Hillman adduct derivatives using chiral diaminophosphine oxides: DIAPHOXs

(Chemical Equation Presented) Asymmetric allylic animation of allylic carbonates prepared from racemic Morita-Baylis-Hillman adducts proceeded in the presence of Pd catalyst, chiral diaminophosphine oxide (DIAPHOX), and BSA, affording the corresponding chiral aza-Morita-Baylis-Hillman adduct derivatives in excellent yield with up to 99% ee. The cyclic reaction products could be converted into various synthetically useful compounds such as chiral cyclic β-amino acids.