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Uridine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-, 3'-acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

142247-31-2

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142247-31-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142247-31-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,2,4 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 142247-31:
(8*1)+(7*4)+(6*2)+(5*2)+(4*4)+(3*7)+(2*3)+(1*1)=102
102 % 10 = 2
So 142247-31-2 is a valid CAS Registry Number.

142247-31-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3'-O-acetyl-5'-O-(4,4'-dimethoxytrityl)-2-deoxyuridine

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:142247-31-2 SDS

142247-31-2Relevant academic research and scientific papers

An anticoagulant with light-triggered antidote activity

Heckel, Alexander,Buff, Maximilian C. R.,Raddatz, Marie-Sophie L.,Mueller, Jens,Poetzsch, Bernd,Mayer, Guenter

, p. 6748 - 6750 (2007/10/03)

(Chemical Equation Presented) A light remedy to overdosing: Aptamers with an intramolecular "caged" antisense region remain active until they are irradiated. Upon irradiation, the antisense activity is released and the aptamer refolds into an inactive str

Commercial-scale synthesis of protected 2′-deoxycytidine and cytidine nucleosides

Divakar, Kikkeri J.,Sawant, Chitra M.,Mulla,Zemse, Deepak V.,Sitabkhan, Sakina M.,Ross, Bruce S.,Sanghvi, Yogesh S.

, p. 1321 - 1325 (2007/10/03)

Transformation of 2′-deoxyuridine and uridine analogs to protected 2′-deoxycytidine and cytidine analogs has been investigated by two different methods. First, traditional triazolation protocol and second p-nitrophenoxylation method. Our studies conclude

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