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2382-64-1

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2382-64-1 Usage

General Description

Uridine, cytidylyl-(3'→5')- is a nucleotide compound involved in the biosynthesis of RNA. It consists of a uridine molecule attached to a cytidine through a phosphodiester bond, resulting in a chain with a 3' and 5' end. Uridine, cytidylyl-(3'®5')- plays a crucial role in the transfer and storage of genetic information in cells, as well as in the production of energy molecules such as adenosine triphosphate (ATP). It is also involved in various cellular processes, including the regulation of cell growth and differentiation. Additionally, uridine, cytidylyl-(3'→5')- has been studied for its potential therapeutic applications in neurodegenerative disorders and cognitive enhancement. Overall, this compound is essential for various biological functions and has potential therapeutic relevance in the field of medicine.

Check Digit Verification of cas no

The CAS Registry Mumber 2382-64-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,8 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2382-64:
(6*2)+(5*3)+(4*8)+(3*2)+(2*6)+(1*4)=81
81 % 10 = 1
So 2382-64-1 is a valid CAS Registry Number.

2382-64-1SDS

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 cytidylyl-(3'->5')-uridine

1.2 Other means of identification

Product number -
Other names Cytidin-Uridin-Dinucleosid

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:2382-64-1 SDS

2382-64-1Upstream product

2382-64-1Relevant articles and documents

Chemical synthesis of RNA via 2′-O-cyanoethylated intermediates

Saneyoshi, Hisao,Ando, Kaori,Seio, Kohji,Sekine, Mitsuo

, p. 11195 - 11203 (2007)

It was found that 2′-O-cyanoethyl group could be removed from 2′-O-cyanoethylated ribonucleoside derivatives by treatment with Bu4NF. This finding was successfully applied to the synthesis of oligoribonucleotides via their 2′-O-cyanoethylated derivatives as key intermediates where a cyanoethyl group was used as the 2′-hydroxyl protecting group. The rate of condensation using this protecting group in the presence of various activators was generally faster than that observed when a TBDMS group was used as the protecting group.

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