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Adenosine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-N-(phenoxyacetyl)-2- [(phenoxyacetyl)amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

156549-48-3

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156549-48-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156549-48-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,5,4 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 156549-48:
(8*1)+(7*5)+(6*6)+(5*5)+(4*4)+(3*9)+(2*4)+(1*8)=163
163 % 10 = 3
So 156549-48-3 is a valid CAS Registry Number.

156549-48-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 5'-O-dimethoxytrityl-N2,N6-bis(phenoxyacetyl)-2,6-diaminopurine 2'-deoxyriboside

1.2 Other means of identification

Product number -
Other names DMT-N2,N6-bisphenoxyacetyl-2'-deoxy-2-aminoadenosine

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:156549-48-3 SDS

156549-48-3Downstream Products

156549-48-3Relevant academic research and scientific papers

Synthesis of oligodeoxyribonucleotides containing 2,6-diaminopurine

Cano,Goodman,Eritja

, p. 501 - 509 (1994)

The preparation of a new protected derivative of 2,6-diaminopurine 2'- deoxyriboside carrying two phenoxyacetyl groups is described. The new derivative is useful to prepare oligonucleotides containing 2,6-diaminopurine and it is deprotected at the same time as the standard protecting groups of the natural bases.

Stabilization of DNA:DNA and DNA/RNA duplexes by substitution of 2'-deoxyadenosine with 2'-deoxy-2-aminoadenosine

Gryaznov,Schultz

, p. 2489 - 2492 (2007/10/02)

Oligonucleotide containing either 2'-deoxyadenosine d(A) or 2'-deoxy-2-aminoadenosine d(A°) were synthesized and their relative binding affinities to complementary DNA and RNA targets compared. Substitution of dA with dA° resulted in sequence- and target-

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