115730-37-5

Basic information

• Product Name: 1,3-Cyclohexanedicarboxylicacid,1-amino-,(1R-cis)-(9CI)
• Synonyms: 1,3-Cyclohexanedicarboxylicacid,1-amino-,(1R-cis)-(9CI)
• CAS NO: 115730-37-5
• Molecular Formula: C₈H₁₃NO₄
• Molecular Weight: 187.19
• Product Categories: AMINOACID
• Mol File: 115730-37-5.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,3-Cyclohexanedicarboxylicacid,1-amino-,(1R-cis)-(9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-Cyclohexanedicarboxylicacid,1-amino-,(1R-cis)-(9CI)(115730-37-5)
• EPA Substance Registry System: 1,3-Cyclohexanedicarboxylicacid,1-amino-,(1R-cis)-(9CI)(115730-37-5)

Safety Data

• Hazardous Substances Data: 115730-37-5(Hazardous Substances Data)

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

This is an alternative name for the compound, which highlights the presence of an amino group and the cyclohexanedicarboxylic acid structure.

Explanation

The compound is derived from cyclohexanedicarboxylic acid, which means it is structurally related and contains additional functional groups.

Explanation

The compound contains an amino group (-NH2), which is an important functional group in organic chemistry and biochemistry.

Explanation

A chiral molecule is one that cannot be superimposed on its mirror image, leading to the existence of enantiomers (mirror-image isomers).

Explanation

The (1R-cis) configuration indicates the specific arrangement of atoms in the molecule, which is important for its stereochemistry and potential biological activity.

Explanation

The compound's unique structure and properties make it a candidate for use in the development of new drugs, materials, and other organic compounds.

Explanation

The compound's properties and potential applications make it relevant to researchers in both chemistry and materials science, as it can contribute to the advancement of knowledge and technology in these fields.

Derivative

Cyclohexanedicarboxylic acid

Amino group

Present

Chiral molecule

Yes

Configuration

(1R-cis)

Potential applications

Pharmaceutical research, synthesis of novel materials and organic compounds

Fields of interest

Chemistry, materials science

Upstream product

• 26629-10-7 2,4-dioxo-1,3-diaza-spiro[4.5]decane-7-carboxylic acid 
• 99407-62-2 (+/-)-isopropyl 3-oxocyclohexanecarboxylate 
• 99438-52-5 (1R,3S)-isopropyl 3-hydroxycyclohexane-1-carboxylate 
• 21531-43-1 (R)-3-oxocyclohexanecarboxylic acid 
• 21531-44-2 (1R)-cis-3-hydroxy-cyclohexanecarboxylic acid 
• 115730-36-4 (1R,3R)-cis-1-amino-1,3-cyclohexanedicarboxylic acid 
• 16205-98-4 3-oxo-cyclohexanecarboxylic acid 
• 37051-56-2 5-Oxo-2-cyclohexenecarboxylic acid 
• 130714-70-4 2,4-Dioxo-1,3-diaza-spiro[4.5]dec-8-ene-7-carboxylic acid 

Relevant articles and documents

Synthesis and resolution of DHCGA, a new conformationally rigid 3,4-dehydroglutamic acid analogue

(±)-1-amino-2-cyclohexene-1,3-dicarboxylic acid (DHCGA),an unsaturated cyclic analogue of glutamic acid, was prepared from 3-carboxy-4-cyclohexenone by a Bucherer-Bergs reaction. Resolution was performed through coupling with L-leucine and separation of the resulting diastereoisomeric dipeptides. Spectral data, including optical rotation and circular dichroism of both enantiomers of DHCGA are reported.