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1,3-Cyclopentanedicarboxylicacid,1-amino-2-methyl-,(1S,2S,3R)-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

207983-48-0

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207983-48-0 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 9 carbon (C), 15 hydrogen (H), 1 nitrogen (N), and 4 oxygen (O) atoms.
2. Amino acid derivative

Explanation

1,3-Cyclopentanedicarboxylicacid,1-amino-2-methyl-,(1S,2S,3R)-(9CI) is derived from an amino acid, which are the building blocks of proteins. It has an amino group (-NH2) and a carboxylic acid group (-COOH) attached to the cyclopentane ring.
3. Cyclopentane ring

Explanation

The compound contains a five-membered carbon ring structure, which is a common structural feature in many organic compounds.
4. Carboxylic acid functional groups

Explanation

The compound has two carboxylic acid groups (-COOH) attached to the cyclopentane ring, which can participate in various chemical reactions, such as esterification and amide formation.
5. Chiral molecule

Explanation

A chiral molecule is one that has non-superimposable mirror images, known as enantiomers. 1,3-Cyclopentanedicarboxylicacid,1-amino-2-methyl-,(1S,2S,3R)-(9CI) has multiple stereoisomers due to the presence of chiral centers.

Explanation

The (1S,2S,3R)-(9CI) designation specifies the stereochemistry of this specific molecule, indicating the spatial arrangement of the atoms around the chiral centers. The "S" and "R" labels denote the absolute configuration of the chiral centers according to the Cahn-Ingold-Prelog priority rules.

Explanation

Due to its unique structure and functional groups, 1,3-Cyclopentanedicarboxylicacid,1-amino-2-methyl-,(1S,2S,3R)-(9CI) may have potential applications in the development of new drugs or as an intermediate in organic synthesis.
8. Context-dependent properties

Explanation

The specific uses and properties of 1,3-Cyclopentanedicarboxylicacid,1-amino-2-methyl-,(1S,2S,3R)-(9CI) may vary depending on its stereochemistry and the context in which it is being utilized, such as in different chemical reactions or biological systems.

Stereochemistry

(1S,2S,3R)-(9CI)

Potential applications

Pharmaceuticals and organic synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 207983-48-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,9,8 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 207983-48:
(8*2)+(7*0)+(6*7)+(5*9)+(4*8)+(3*3)+(2*4)+(1*8)=160
160 % 10 = 0
So 207983-48-0 is a valid CAS Registry Number.

207983-48-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,2S,3R)-1-amino-2-methylcyclopentane-1,3-dicarboxylic acid

1.2 Other means of identification

Product number -
Other names 1,3-Cyclopentanedicarboxylicacid,1-amino-2-methyl-,(1S,2S,3R)

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:207983-48-0 SDS

207983-48-0Upstream product

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