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118374-59-7

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  • Cytidine, 5'?P''-ester with thiotriphosphoricacid ((HO)2P(O)OP(O)(OH)OP(O)(OH)(SH)), (R)- (9CI)

    Cas No: 118374-59-7

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  • CYTIDINE-5'-O-(1-THIOTRIPHOSPHATE), RP-ISOMER SODIUM SALT

    Cas No: 118374-59-7

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118374-59-7 Usage

Description

CYTIDINE-5'-O-(1-THIOTRIPHOSPHATE), RP-ISOMER SODIUM SALT is a nucleotide analog used in biochemical and molecular biological research, featuring a specific stereochemistry that allows incorporation into RNA during transcription for studying RNA synthesis and processing.

Uses

Used in Biochemical Research:
CYTIDINE-5'-O-(1-THIOTRIPHOSPHATE), RP-ISOMER SODIUM SALT is used as a research tool for investigating RNA synthesis and processing, providing insights into the mechanisms of RNA biology.
Used in Molecular Biology:
In molecular biology, CYTIDINE-5'-O-(1-THIOTRIPHOSPHATE), RP-ISOMER SODIUM SALT is used as a component in experiments aiming to understand the role of RNA in various biological processes, including gene expression and regulation.
Used in Laboratory Settings:
The sodium salt form of CYTIDINE-5'-O-(1-THIOTRIPHOSPHATE), RP-ISOMER is commonly used in laboratories due to its increased stability and solubility, facilitating its application in a wide range of experiments and analyses.

Check Digit Verification of cas no

The CAS Registry Mumber 118374-59-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,3,7 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 118374-59:
(8*1)+(7*1)+(6*8)+(5*3)+(4*7)+(3*4)+(2*5)+(1*9)=137
137 % 10 = 7
So 118374-59-7 is a valid CAS Registry Number.

118374-59-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Tetrasodium 4-amino-1-[5-O-(oxido{[(phosphonatooxy)phosphinato]ox y}phosphorothioyl)-β-D-arabinofuranosyl]-2(1H)-pyrimidinone

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:118374-59-7 SDS

118374-59-7Upstream product

118374-59-7Downstream Products

118374-59-7Relevant articles and documents

Rapid and Efficient Synthesis of Nucleoside 5'-O-(1-Thiotriphosphates), 5'-Triphosphates and 2',3'-Cyclophosphorothioates Using 2-Chloro-4H-1,3,2-benzodioxaphosphorin-4-one

Ludwig, Janos,Eckstein, Fritz

, p. 631 - 635 (2007/10/02)

2-Chloro-4H-1,3,2-benzodioxaphosphorin-4-one phosphitylates the 5'-hydroxy group of a nucleoside to form an intermediate (2), which on subsequent reaction with pyrophosphate produces, in a double displacement process, a P2,P3-dioxo-P1-5'-nucleosidylcyclotriphophite (3).Oxidation with sulfur gives a nucleoside 5'-(1-thiocyclotriphosphate) (4), which is hydrolyzed to the diastereomeric mixture of a nucleoside 5'-O-(1-thiotriphosphate) (5).Alternatively, 3 can be oxidized with iodine/water to furnish nucleoside 5'-triphosphates 6.This reagent can also be applied to the synthesis of nucleoside 2',3'-cyclic phosphorothioates.Protection of nucleobase functional groups is not required.

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