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1,3-Dioxolane-4-carboxylic acid, 5-methyl-2-[(phenylmethoxy)methyl]-, (2R,4S,5R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

501013-48-5

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501013-48-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 501013-48-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,0,1 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 501013-48:
(8*5)+(7*0)+(6*1)+(5*0)+(4*1)+(3*3)+(2*4)+(1*8)=75
75 % 10 = 5
So 501013-48-5 is a valid CAS Registry Number.

501013-48-5SDS

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 (2R,4S,5R)-2-benzyloxymethyl-5-methyl-1,3-dioxolane-4-carboxylic acid

1.2 Other means of identification

Product number -
Other names (2R,4S,5R)-2-Benzyloxymethyl-5-methyl-[1,3]dioxolane-4-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:501013-48-5 SDS

501013-48-5Relevant academic research and scientific papers

Synthesis and biological evaluation of 5R- and 5S-methyl substituted D- and L-configuration 1,3-dioxolane nucleoside analogs

Bera, Sanjib,Malik, Leila,Bhat, Balkrishen,Carroll, Steven S.,Hrin, Renee,MacCoss, Malcolm,McMasters, Daniel R.,Miller, Michael D.,Moyer, Greg,Olsen, David B.,Schleif, William A.,Tomassini, Joanne E.,Eldrup, Anne B.

, p. 6237 - 6247 (2007/10/03)

1,3-Dioxolane and 1,3-oxathiolane nucleoside analogs play an important role in anti-viral and anti-neoplastic chemotherapy. We report here the synthesis of 2-hydroxymethyl-5-methyl-1,3-dioxolanylpurine nucleosides from 4-acetoxy-2-(benzyloxymethyl)-5-meth

Synthesis and evaluation of optically pure dioxolanes as inhibitors of hepatitis C virus RNA replication

Bera, Sanjib,Malik, Leila,Bhat, Balkrishen,Carroll, Steven S.,MacCoss, Malcolm,Olsen, David B.,Tomassini, Joanne E.,Eldrup, Anne B.

, p. 4455 - 4458 (2007/10/03)

A series of optically pure 1,3-dioxolane nucleoside mimics was synthesized by a synthetic route that allowed incorporation of a 5R-methyl substituent from commercially available starting materials. The pyrrolo[2,3-d]pyrimidine heterocycle was chosen as a

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