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129681-71-6

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129681-71-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129681-71-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,6,8 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 129681-71:
(8*1)+(7*2)+(6*9)+(5*6)+(4*8)+(3*1)+(2*7)+(1*1)=156
156 % 10 = 6
So 129681-71-6 is a valid CAS Registry Number.

129681-71-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2'-O-tert-butyldimethylsilyl-5'-O-(4,4'-dimethoxytrityl)-6-N-benzoyladenosine

1.2 Other means of identification

Product number -
Other names 5'-O-DMT-N-benzoyl-2'-O-TBDMS-adenosine

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:129681-71-6 SDS

129681-71-6Relevant articles and documents

CYCLIC DINUCLEOTIDE COMPOUND AND USES THEREOF

-

Paragraph 0101-0108, (2021/11/05)

Provided are a compound of formula (I), an optical isomer thereof, a pharmaceutically acceptable salt thereof, uses of said compound acting as a STING agonist.

CYCLIC DI-NUCLEOTIDE COMPOUNDS AND METHODS OF USE

-

, (2017/10/11)

Disclosed are cyclic-di-nucleotide cGAMP analogs, methods of synthesizing the compounds, pharmaceutical compositions comprising the compounds thereof, and use of compounds and compositions in medical therapy.

Synthesis of 2'-O-substituted ribonucleosides.

Serebryany,Beigelman

, p. 1007 - 1009 (2007/10/03)

An efficient synthesis of 2'-O-substituted ribonucleosides, including 2'-O-TBDMS and 2'-O-TOM protected as well as 2'-O-Me and 2'-O-allyl derivatives is presented. Di-t-butylsilylene group was employed for simultaneous protection of 3'- and 5'- hydroxyl functions of nucleoside on the first step. Subsequent silylation or alkylation of free 2'-OH followed by introduction of suitable protection on the base moiety and removal of cyclic silyl protection gave target compounds in a high yield.

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