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184763-07-3

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184763-07-3 Usage

Type of compound

Derivative of azetidinecarboxylic acid

Structure

Heterocyclic compound with a four-membered ring and a carboxylic acid group

Common use

Building block in the synthesis of peptide and protein molecules

Synthesis method

Solid-phase peptide synthesis

Protecting group

FMoc (9-fluorenylmethoxycarbonyl)

Protecting group purpose

To protect the amine group of the azetidinecarboxylic acid

Deprotection

Selective deprotection under mild conditions

Field of interest

Medicinal chemistry and pharmaceutical research

Application

Modification and manipulation of peptide structures for various applications

Check Digit Verification of cas no

The CAS Registry Mumber 184763-07-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,7,6 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 184763-07:
(8*1)+(7*8)+(6*4)+(5*7)+(4*6)+(3*3)+(2*0)+(1*7)=163
163 % 10 = 3
So 184763-07-3 is a valid CAS Registry Number.

184763-07-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(9-fluorenylmethyloxycarbonyl)-azetidine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-(fluorenylmethoxycarbonyl)azetidine-2(S)-carboxylic acid

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:184763-07-3 SDS

184763-07-3Upstream product

184763-07-3Relevant 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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