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22738-07-4

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22738-07-4 Usage

Chemical classification

Aminosugar

Molecular structure

Derived from xylose, with an amino group attached at the second carbon atom

Biological relevance

Found in the structural components of various biological molecules, including glycoproteins, glycosaminoglycans, and proteoglycans

Role

Crucial in the formation and function of complex molecules, as well as in regulating cellular processes

Therapeutic potential

Studied for potential applications in treating genetic metabolic disorders and inflammatory diseases

Overall significance

Important chemical compound with notable biological relevance and potential pharmacological value

Check Digit Verification of cas no

The CAS Registry Mumber 22738-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,7,3 and 8 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 22738-07:
(7*2)+(6*2)+(5*7)+(4*3)+(3*8)+(2*0)+(1*7)=104
104 % 10 = 4
So 22738-07-4 is a valid CAS Registry Number.

22738-07-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-2-deoxy-D-xylose

1.2 Other means of identification

Product number -
Other names 2-Amino-2-deoxy-D-xylose

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:22738-07-4 SDS

22738-07-4Upstream product

22738-07-4Downstream Products

22738-07-4Relevant articles and documents

Process for the preparation of cyclopropane carboxylic acid esters

-

, (2008/06/13)

3-(Halogenovinyl- or propenyl-)-2,2-dimethyl cyclopropane-1-carboxylic acid esters, which are precursors of, or may themselves be, pyrethroid insecticides, are prepared by the reaction of certain halogenopentadienes with an alkyl diazoacetate in the presence of a catalyst which is a transition metal complex of certain chiral Schiff bases, which catalysts tend to increase the yield of preferred cis IR isomer relative to the other possible isomers.

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