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METHYL-2-DEOXY-5-O-PIVALOYL-ALPHA-D-ERYTHRO-PENTOFURANOSIDE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

138147-15-6

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138147-15-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 138147-15-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,1,4 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 138147-15:
(8*1)+(7*3)+(6*8)+(5*1)+(4*4)+(3*7)+(2*1)+(1*5)=126
126 % 10 = 6
So 138147-15-6 is a valid CAS Registry Number.

138147-15-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name METHYL-2-DEOXY-5-O-PIVALOYL-α-D-ERYTHRO-PENTOFURANOSIDE

1.2 Other means of identification

Product number -
Other names -

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:138147-15-6 SDS

138147-15-6Downstream Products

138147-15-6Relevant academic research and scientific papers

Decitabine intermediate compound VI

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Paragraph 0025; 0091-0101, (2021/01/24)

The invention belongs to the technical field of chemical synthesis, and provides a decitabine intermediate compound. A preparation route of the decitabine intermediate compound comprises the followingsteps: taking an oxymethyl compound of a hydroxyl group at a 1 site of 2-deoxy-D-ribose as a raw material, protecting a hydroxyl group at a 3 site and a hydroxyl group at a 5 site respectively, then performing acetylation substitution on a 1 site of sugar, and further treating to obtain the compound. The method is simple and convenient to operate, does not need special equipment, is good in product purity and high in yield, and is suitable for industrial production; decitabine is further synthesized by utilizing the compound, so that the stereoselectivity is high, and the purity isgood.

Process for the manufacture of 2-deoxy-D-threo-pentofuranosides, intermediates for their manufacture and their use

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, (2008/06/13)

Disclosed is a process for the manufacture of 2-Deoxy-D-threo-pentofuranosides of formula 1 wherein R1 is an alkyl group having 1 to 4 carbon atoms and R7 is a hydroxy protection group by reacting a 2-deoxy-D-erythro-pentofuranoside of formula 2 wherein R1 is an alkyl group having 1 to 4 carbon atoms, R3 is an alkyl-, aryl-, alkylaryl- or aralkyl-sulfonyl group, either unsubstituted or substituted one or more times by halogen atoms, nitro or alkoxy groups, an imidazolesulfonyl or halosulfonyl group, and R4 has the same meaning as R3 or signifies a hydroxy protection group. Furtheron disclosed are a process for the manufacture of 3-substituted 2-deoxy-D-erythro-pentofuranosides using these compounds and novel and substituted and unsubstituted 2-deoxy-D-pentofuranosides and their use for the manufacture of 3'-substituted 2'-deoxynucleosides.

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