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52571-45-6

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  • China Biggest Factory Manufacturer Supply N4-BENZOYL-2'-O-METHYLCYTIDINE CAS 52571-45-6

    Cas No: 52571-45-6

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52571-45-6 Usage

Uses

N4-Benzoyl-2’-O-methylcytidine is a key building block in the block synthesis strategy of tRNA fragments.

Check Digit Verification of cas no

The CAS Registry Mumber 52571-45-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,5,7 and 1 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 52571-45:
(7*5)+(6*2)+(5*5)+(4*7)+(3*1)+(2*4)+(1*5)=116
116 % 10 = 6
So 52571-45-6 is a valid CAS Registry Number.
InChI:InChI=1/C17H19N3O6/c1-25-14-13(22)11(9-21)26-16(14)20-8-7-12(19-17(20)24)18-15(23)10-5-3-2-4-6-10/h2-8,11,13-14,16,21-22H,9H2,1H3,(H,18,19,23,24)

52571-45-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N4-Benzoyl-2'-O-methylcytidine

1.2 Other means of identification

Product number -
Other names N-[1-[(2R,3R,4R,5R)-4-hydroxy-5-(hydroxymethyl)-3-methoxyoxolan-2-yl]-2-oxopyrimidin-4-yl]benzamide

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:52571-45-6 SDS

52571-45-6Relevant articles and documents

Process for the preparation of 2'-O-alkyl purine phosphoramidites

-

, (2016/06/29)

2'-O-alkylated guanosine, uridine, cytidine, and 2,6-diaminopurine 3'-O-phosphoramidites are prepared by alkylating nucleoside precursors, adding suitable blocking groups and phosphitylating. Alkylation is effected on 2,6-diamino-9-(β-D-ribofuranosyl)purine followed by deamination to prepare guanosine 2'-O-alkylated 3'-O-phosphormidites. Alkylation is effected on a dialkyl stannylene derivative of uridine to prepare uridine 2'-O-alkylated 3'-O-phosphormidites. Alkylation is effected directly on cytidine to prepare cytidine 2'-O-alkylated 3'-O-phosphormidites. Alkylation is effected directly on 2,6-diaminopurine to prepare 2,6-diaminopurine 2'-O-alkylated 3'-O-phosphormidites.

SYNTHESIS OF N,O-PROTECTED DERIVATIVES OF 2'-O-METHYLCYTIDINE AND OF 2'-O-METHYL- AND N1-METHYLGUANOSINES

Gladkaya, V. A.,Levitskaya, Z. V.,Shalamai, A. S.,Usenko, L. S.,Dashevskaya, T. A.

, p. 488 - 492 (2007/10/02)

Using selective 3',5'-O-tetraisopropyldisiloxane protection, N-acyl-2'-O-methyl derivatives of cytidine and guanosine and of 2'-O-tetrahydropyranyl-N1-methyl-guanosine have been synthesized.It has been shown that the spatial screening of the am

5'-O-Trityl Group Promoted Directive Effect in the Preparation of 2'-O-Methylribonucleosides

Heikkilae, Jarmo,Bjoerkman, Sven,Oeberg, Bo,Chattopadhyaya, Jyoti

, p. 715 - 718 (2007/10/02)

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