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13089-48-0

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13089-48-0 Usage

Chemical Properties

Slightly Pink Solid

Uses

Different sources of media describe the Uses of 13089-48-0 differently. You can refer to the following data:
1. N4-Benzoylcytidine is a useful building block for oligoribonucleotide synthesis
2. N-Benzoylcytidine is a useful building block for oligoribonucleotide synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 13089-48-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,8 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13089-48:
(7*1)+(6*3)+(5*0)+(4*8)+(3*9)+(2*4)+(1*8)=100
100 % 10 = 0
So 13089-48-0 is a valid CAS Registry Number.
InChI:InChI=1/C16H17N3O6/c20-8-10-12(21)13(22)15(25-10)19-7-6-11(18-16(19)24)17-14(23)9-4-2-1-3-5-9/h1-7,10,12-13,15,20-22H,8H2,(H,17,18,23,24)/t10-,12-,13-,15-/m1/s1

13089-48-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Detail
  • TCI America

  • (B3094)  N4-Benzoylcytidine  >98.0%(HPLC)(T)

  • 13089-48-0

  • 1g

  • 790.00CNY

  • Detail
  • TCI America

  • (B3094)  N4-Benzoylcytidine  >98.0%(HPLC)(T)

  • 13089-48-0

  • 5g

  • 2,450.00CNY

  • Detail
  • Aldrich

  • (326151)  N4-Benzoylcytidine  99%

  • 13089-48-0

  • 326151-1G

  • 1,146.60CNY

  • Detail

13089-48-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name N-Benzoylcytidine

1.2 Other means of identification

Product number -
Other names N4-BENZOYL-D-CYTIDINE

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:13089-48-0 SDS

13089-48-0Downstream Products

13089-48-0Relevant articles and documents

Microwaves - A powerful tool for the base protection of cytidine

Nahar, Pradip

, p. 7253 - 7254 (1997)

Use of microwaves for the base protection of cytidine is described. The procedure gives N-acylcytidine in nearly quantitative yield in 40-60 seconds.

Synthesis method for azvudine

-

Paragraph 0079-0081, (2020/11/22)

The invention discloses a synthesis method for azvudine. The method comprises the following steps of carrying out a hydroxyl substitution reaction on a compound 4 and an iodine elementary substance toobtain a compound 5, carrying out an elimination reaction on an iodo group in the compound 5 to obtain a compound 6, reacting the compound 6 with azide under the catalysis of ICl to obtain a compound7, carrying out an iodine substitution reaction on the compound 7 and carboxylic acid to obtain a compound 8, and carrying out an amino and hydroxyl deprotection reaction on the compound 8 to obtaina compound 9, namely the alzvudine. Compared with an existing synthesis method, the synthesis method has the advantages of short synthesis route, shortened reaction time, mild reaction conditions andeasily controlled reaction process, can be used for preparing the alzvudine with the lower cost, and has a very good application prospect.

New tools in nucleoside toolbox of tick-borne encephalitis virus reproduction inhibitors

Orlov, Alexey A.,Drenichev, Mikhail S.,Oslovsky, Vladimir E.,Kurochkin, Nikolay N.,Solyev, Pavel N.,Kozlovskaya, Liubov I.,Palyulin, Vladimir A.,Karganova, Galina G.,Mikhailov, Sergey N.,Osolodkin, Dmitry I.

supporting information, p. 1267 - 1273 (2017/06/19)

Design and development of nucleoside analogs is an established strategy in the antiviral drug discovery field. Nevertheless, for many viruses the coverage of structure-activity relationships (SAR) in the nucleoside chemical space is not sufficient. Here we present the nucleoside SAR exploration for tick-borne encephalitis virus (TBEV), a member of Flavivirus genus. Promising antiviral activity may be achieved by introduction of large hydrophobic substituents in the position 6 of adenosine or bulky silyl groups to the position 5′. Introduction of methyls to the ribose moiety does not lead to inhibition of TBEV reproduction. Possible mechanisms of action of these nucleosides include the inhibition of viral entry or interaction with TBEV non-structural protein 5 methyltransferase or RNA-dependent RNA polymerase domains.

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