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2-Azetidinecarboxylic acid, hydrochloride, (2R)is a hydrochloride salt of (2R)-2-Azetidinecarboxylic acid, an organic compound characterized by a four-membered ring and a carboxylic acid functional group. The (2R) configuration denotes its stereochemistry, which is crucial for its biological activity and interactions with other molecules. This versatile compound is widely used in the pharmaceutical and chemical industries.

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  • 647854-72-6 Structure
  • Basic information

    1. Product Name: 2-Azetidinecarboxylic acid, hydrochloride, (2R)-
    2. Synonyms: 2-Azetidinecarboxylic acid, hydrochloride, (2R)-;(R)-Azetidine-2-carboxylic acid hydrochloride;R-2-Azetidinecarboxylic acid hydrochloride
    3. CAS NO:647854-72-6
    4. Molecular Formula: C4H8ClNO2
    5. Molecular Weight: 137.56482
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 647854-72-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: Inert atmosphere,Room Temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Azetidinecarboxylic acid, hydrochloride, (2R)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Azetidinecarboxylic acid, hydrochloride, (2R)-(647854-72-6)
    11. EPA Substance Registry System: 2-Azetidinecarboxylic acid, hydrochloride, (2R)-(647854-72-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 647854-72-6(Hazardous Substances Data)

647854-72-6 Usage

Uses

Used in Pharmaceutical Industry:
2-Azetidinecarboxylic acid, hydrochloride, (2R)is used as a building block for the synthesis of peptides and pharmaceuticals. Its unique structure and stereochemistry make it a valuable component in the development of new drugs with specific therapeutic properties.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2-Azetidinecarboxylic acid, hydrochloride, (2R)is utilized for its potential applications in the discovery and optimization of novel bioactive molecules. Its unique structural features and stereochemistry allow for the design of compounds with improved binding affinity, selectivity, and pharmacokinetic properties.
Overall, 2-Azetidinecarboxylic acid, hydrochloride, (2R)is a promising compound with diverse applications in the pharmaceutical and chemical industries, offering opportunities for the development of innovative therapeutic agents and chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 647854-72-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,4,7,8,5 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 647854-72:
(8*6)+(7*4)+(6*7)+(5*8)+(4*5)+(3*4)+(2*7)+(1*2)=206
206 % 10 = 6
So 647854-72-6 is a valid CAS Registry Number.

647854-72-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-Azetidine-2-carboxylic acid hydrochloride

1.2 Other means of identification

Product number -
Other names (2R)-azetidine-2-carboxylic acid,hydrochloride

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:647854-72-6 SDS

647854-72-6Upstream product

647854-72-6Downstream Products

647854-72-6Relevant articles and documents

Methods for producing N-protected-azetidine-2-carboxylic acids

-

, (2008/06/13)

There is disclosed a method for producing an essentially enantiomerically pure N-protected-azetidine-2-carboxylic acid of formula (1): which method is characterized by: subjecting a crude enantiomerically excess N-protected-azetidine-2-carboxylic acid comprising said enantiomer represented by formula (1) in excess to the other enantiomer thereof to crystallization in an organic solvent selected from aromatic hydrocarbon, aliphatic ether, aliphatic alcohol, aliphatic ketone, aliphatic nitrile, aliphatic amide, aliphatic sulfoxide, aliphatic ester and a mixed solvent thereof, wherein R is: an optionally substituted alkyl, alicyclic or alicyclicalkyl group, an optionally substituted alkenyl group, an optionally substituted aryl group, an optionally substituted heteroaryl group, or a dialkylamino group, and absolute configuration of the asterisked asymmetric carbon atom is S or R.

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