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4-amino-1-(2-deoxyhexopyranosyl)pyrimidin-2(1H)-one, also known as 2'-deoxycytidine, is a nucleoside composed of a pyrimidine base (cytosine) attached to a 2'-deoxyribose sugar. 4-amino-1-(2-deoxyhexopyranosyl)pyrimidin-2(1H)-one is a key component of DNA, as it pairs with guanine through hydrogen bonding, playing a crucial role in the storage and transmission of genetic information. 2'-deoxycytidine is an essential building block for the synthesis of DNA, and its proper functioning is vital for maintaining the integrity of genetic material.

6027-65-2

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6027-65-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6027-65-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,2 and 7 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6027-65:
(6*6)+(5*0)+(4*2)+(3*7)+(2*6)+(1*5)=82
82 % 10 = 2
So 6027-65-2 is a valid CAS Registry Number.

6027-65-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-CHLOROCYTOSINE ARABINO-SIDE

1.2 Other means of identification

Product number -
Other names 5-chlorocytosine arabinoside*crystalline

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

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More Details:6027-65-2 SDS

6027-65-2Downstream Products

6027-65-2Relevant academic research and scientific papers

Synthesis, Structure, and Biological Activity of Certain 2-Deoxy-β-D-ribo-hexopyranosyl Nucleosides and Nucleotides

Nord, L. Dee,Dalley, N. Kent,McKernan, Patricia A.,Robins, Roland K.

, p. 1044 - 1054 (2007/10/02)

2-Deoxy-β-D-ribo-hexopyranosyl nucleosides with adenine (2), hypoxanthine (17), guanine (23), cytosine (13), and uracil (7) as the aglycon were synthesized by the Lewis-acid-catalyzed condensation of an appropriate trimethylsilylated heterocyclic base and

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