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esterbut-6 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

125161-48-0

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125161-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 125161-48-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,1,6 and 1 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 125161-48:
(8*1)+(7*2)+(6*5)+(5*1)+(4*6)+(3*1)+(2*4)+(1*8)=100
100 % 10 = 0
So 125161-48-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H22O7/c1-4-5-8(15)17-6-7(14)10-9(16)11-12(18-10)20-13(2,3)19-11/h7,9-12,14,16H,4-6H2,1-3H3/t7-,9+,10-,11-,12-/m1/s1

125161-48-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2R)-2-[(3aR,5R,6S,6aR)-6-hydroxy-2,2-dimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl]-2-hydroxyethyl] butanoate

1.2 Other means of identification

Product number -
Other names Monobut-6

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:125161-48-0 SDS

125161-48-0Downstream Products

125161-48-0Relevant academic research and scientific papers

Preparation and biological evaluation of some 1,2-O-isopropylidene-D- hexofuranose esters

Catelani, Giorgio,D'Andrea, Felicia,Landi, Martina,Zuccato, Cristina,Bianchi, Nicoletta,Gambari, Roberto

, p. 538 - 544 (2007/10/03)

The synthesis and biological evaluation of some new glycose esters bearing the 1,2-O-isopropylidene-D-hexofuranose functionality and belonging to the 3-O-acyl-D-allose and 6-O-acyl-D-glucose series are reported. When the results concerning cell growth inh

SYNTHESIS OF MONOESTERS AS SURFACTANTS AND DRUGS FROM D-GLUCOSE

Goueth, Pierre Y.,Gogalis, Pascalis,Bikanga, Raphael,Gode, Paul,Postel, Denis,et al.

, p. 249 - 272 (2007/10/02)

We have synthesized a series of monoesters from D-glucose corresponding to the structures 3-O-acyl, 6-O-acyl-1,2-O-isopropylidene-α-D-glucofuranose and 3-acyl-D-glucose, following the sequence of reactions : D-glucose -> diacetone glucose -> acylation -> partial or total deprotection.These compounds were prepared as either potential non-ionic surfactants (fatty acid esters and perfluoroalkylated ester) or antitumour drugs (n-butyric esters).Results concerning surface activity, toxicity and antitumour effects are reported.A novel method for obtaining partially deprotected 6-O-acyl esters from their corresponding 3-O-acyl isomers is reported.Deprotection conditions have been studied and a higher selectivity in partial deprotection has been achieved.We have given particular attention to the choice of solvents and reagents in order not to limit the extent to which the products might be applied.

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