209460-85-5

Basic information

• Product Name: (R)-AMINO-4-HYDROXY-CYCLOHEXANEACETIC ACID
• Synonyms: (R)-AMINO-4-HYDROXY-CYCLOHEXANEACETIC ACID
• CAS NO: 209460-85-5
• Molecular Formula: C₈H₁₅NO₃
• Molecular Weight: 173.21
• Mol File: 209460-85-5.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (R)-AMINO-4-HYDROXY-CYCLOHEXANEACETIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-AMINO-4-HYDROXY-CYCLOHEXANEACETIC ACID(209460-85-5)
• EPA Substance Registry System: (R)-AMINO-4-HYDROXY-CYCLOHEXANEACETIC ACID(209460-85-5)

Safety Data

• Hazardous Substances Data: 209460-85-5(Hazardous Substances Data)

Usage

Description

(R)-AMINO-4-HYDROXY-CYCLOHEXANEACETIC ACID, also known as (R)-HACA, is a chiral chemical compound derived from cyclohexaneacetic acid. It features an amino group and a hydroxy group attached to a cyclohexane ring, giving it unique structural properties. As a chiral molecule, it exists in two enantiomers, (R)-HACA and (S)-HACA, which are mirror images of each other. (R)-AMINO-4-HYDROXY-CYCLOHEXANEACETIC ACID has garnered interest in the scientific community for its potential pharmacological properties and its role as a building block in the development of pharmaceutical drugs. Additionally, it has been investigated for its applications in the synthesis of various chemical compounds and in the study of chiral chemistry.

Uses

Used in Pharmaceutical Development:
(R)-AMINO-4-HYDROXY-CYCLOHEXANEACETIC ACID is used as a building block for the development of pharmaceutical drugs due to its unique structure and potential pharmacological properties.
Used in Chemical Synthesis:
(R)-AMINO-4-HYDROXY-CYCLOHEXANEACETIC ACID is used as an intermediate in the synthesis of various chemical compounds, contributing to the diversity of chemical products.
Used in Chiral Chemistry Research:
(R)-AMINO-4-HYDROXY-CYCLOHEXANEACETIC ACID is used as a subject of study in chiral chemistry, helping researchers understand the behavior and properties of chiral molecules and their interactions with other compounds.

Upstream product

• 22818-40-2 D-4-hydroxyphenylglycine 

Downstream Products

• 130624-89-4 trans-(D)-N^α-(Boc)-4-hydroxycyclohexylglycine 
• 130624-89-4 cis-(D)-N^α-(Boc)-4-hydroxycyclohexylglycine 
• 130624-90-7 trans-(D)-N^α-(Boc)-4-hydroxycyclohexylglycine benzyl ester 
• 130624-90-7 cis-(D)-N^α-(Boc)-4-hydroxycyclohexylglycine benzyl ester 
• 91675-87-5 (2R)-2-Benzamido-2-(4-hydroxycyclohexyl)acetic Acid 
• 362621-38-3 (R)-(4-Hydroxy-cyclohexyl)-(4'-methoxy-biphenyl-4-sulfonylamino)-acetic acid 
• 369598-85-6 Methyl (R)-N-{[4'-Methoxy-(1,1'-biphenyl)-4-yl]-sulfonyl}-amino-(4-oxocyclohex-1-yl)-acetate 
• 369656-86-0 Methyl (R)-N-{[4'-Methoxy-(1,1'-biphenyl)-4-yl]-sulfonyl}-amino-(4-hydroxy-cyclohex-1-yl)-acetate 
• 586377-12-0 Methyl (R)-N-{[4'-Methoxy-(1,1'-biphenyl)-4-yl]-sulfonyl}-amino-(1,5-dioxa-spiro[5.5]undec-9-yl)-acetate 
• 586958-75-0 Methyl (R)-N-{[4'-Methoxy-(1,1'-biphenyl)-4-yl]-sulfonyl}-amino-[4-(N-benzyl-amino)-cyclohex-1-yl]-acetate 
• 91740-53-3 (2R)-2-Benzamido-2-(4-oxocyclohexyl)acetic Acid 
• 91740-54-4 (2R)-2-Benzamido-2-(4-oximinocyclohexyl)acetic Acid 
• 126455-20-7 cis-(D)-4-guanidinocyclohexylglycine 
• 130624-88-3 trans-(D)-4-hydroxycyclohexylglycine benzyl ester 

Relevant articles and documents

Carbocyclic side chain containing, N-substituted metalloprotease inhibitors

The compounds have a structure according to the following Formula (I): are effective in treating conditions characterized by excess activity of metalloprotease enzymes.

Synthesis of Optically Pure Analogue of D-Arginine Methyl Ester with Antiarrhythmic Activity

The synthesis of the methyl esters of optically pure trans and cis 4-guanidinocyclohexylglycine as rigid analogues of D-arginine methyl ester are described.