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139239-73-9

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139239-73-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 139239-73-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,2,3 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 139239-73:
(8*1)+(7*3)+(6*9)+(5*2)+(4*3)+(3*9)+(2*7)+(1*3)=149
149 % 10 = 9
So 139239-73-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H26NO10P/c14-11(13(18)19)9-24-25(20,21)23-8-10(15)7-22-6-4-2-1-3-5-12(16)17/h10-11,15H,1-9,14H2,(H,16,17)(H,18,19)(H,20,21)/t10-,11+/m1/s1

139239-73-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-[(2R)-3-[[(2S)-2-amino-2-carboxyethoxy]-hydroxyphosphoryl]oxy-2-hydroxypropoxy]heptanoic acid

1.2 Other means of identification

Product number -
Other names 7-[(2R)-3-[[(2S)-2-amino-3-hydroxy-3-oxopropoxy]-hydroxyphosphoryl]oxy-2-hydroxypropoxy]heptanoic 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

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

More Details:139239-73-9 SDS

139239-73-9Downstream Products

139239-73-9Relevant articles and documents

Synthesis of new ether glycerophospholipids structurally related to modulator

Garcia,Pascual,Borras,Andreu,Fos,Mauleon,Carganico,Arcamone

, p. 10023 - 10034 (1991)

A series of new glycerophospholipids, bearing a short-chain carboxylic acid in position sn-1 and phosphocholine or phosphoserine in postion sn-3 of glycerol, have been prepared in good overall yields. Compound 11, 1-0-(6-carboxyhexyl)-sn-glycero-3-phosphoserine, a strict analog of the structure proposed for modulator, has been synthesized in a stereoselective way from (R)-1,2-isopropylideneglycerol 1.

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