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2'-deoxycytidine 3',5'-diphosphate, also known as dCDP, is a nucleotide composed of a deoxycytidine base attached to a ribose sugar, which is further linked to two phosphate groups. 2'-deoxycytidine 3',5'-diphosphate plays a crucial role in DNA synthesis as it is an intermediate in the conversion of deoxycytidine to deoxycytidine triphosphate (dCTP), a key building block for DNA. dCDP is formed through the phosphorylation of deoxycytidine monophosphate (dCMP) by nucleoside diphosphate kinases, and it can be further phosphorylated to dCTP by nucleoside diphosphate kinases or ribonucleotide reductases. The regulation of dCDP levels is essential for maintaining the balance of nucleotide pools and ensuring proper DNA replication and repair processes within cells.

4682-43-3

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4682-43-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4682-43-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,8 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4682-43:
(6*4)+(5*6)+(4*8)+(3*2)+(2*4)+(1*3)=103
103 % 10 = 3
So 4682-43-3 is a valid CAS Registry Number.

4682-43-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [(2R,3S,5R)-5-(4-amino-2-oxopyrimidin-1-yl)-2-(phosphonooxymethyl)oxolan-3-yl] dihydrogen phosphate

1.2 Other means of identification

Product number -
Other names 2'-Pdcp

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:4682-43-3 SDS

4682-43-3Downstream Products

4682-43-3Relevant academic research and scientific papers

Solid-phase enzymatic synthesis of oligonucleotides.

Schmitz,Reetz

, p. 1729 - 1731 (2008/02/11)

[formula: see text] The controlled and selective synthesis of oligonucleotides on the solid phase is possible under mild aqueous conditions using the enzyme T4 RNA ligase, the resins being tentagel or kieselguhr/polydimethylacrylamide.

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