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Uridine 5'-(benzoylamino)-5'-deoxy- is a chemical compound with the molecular formula C16H17N3O6. It is a derivative of uridine, a nucleoside composed of uracil and ribose, where the 5'-hydroxyl group of the ribose sugar is replaced by a benzoylamino group. This modification results in a change in the chemical properties and potential biological activities of the compound. It is often used in research and development for studying the effects of such modifications on the structure and function of nucleic acids and their interactions with proteins. The compound may also have potential applications in the development of new therapeutic agents targeting nucleic acid metabolism or related pathways.

61210-33-1

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61210-33-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61210-33-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,2,1 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61210-33:
(7*6)+(6*1)+(5*2)+(4*1)+(3*0)+(2*3)+(1*3)=71
71 % 10 = 1
So 61210-33-1 is a valid CAS Registry Number.

61210-33-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[[(2R,3S,4R,5R)-5-(2,4-dioxopyrimidin-1-yl)-3,4-dihydroxyoxolan-2-yl]methyl]benzamide

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:61210-33-1 SDS

61210-33-1Relevant academic research and scientific papers

Combining a solution-phase derived library with in-situ cellular bioassay: Prompt screening of amide-forming minilibraries using MTT assay

Chiang, Li-Wu,Pei, Kai,Chen, Shao-Wei,Huang, Ho-Lien,Lin, Kun-Ju,Yen, Tzu-Chen,Yu, Chung-Shan

experimental part, p. 714 - 718 (2009/12/29)

We constructed a minilibrary using a solution-phase synthesis through coupling of three core amino compounds (5′-amino-5′-deoxy uridine, 5′-amino-2′,5′-di-deoxy arabinosyl uridine, and butan-1-amine) with 30 carboxylic acids via amide bond formation. The

Stereochemical Transformations of 5'-Amino-5'-deoxyuridine and Its 5,6-Dihydro-analogue. 5'-N-Aminoacyl Derivatives of 5'-Amino-5'-deoxy-5,6-dihydrouridine

Skaric, Vinko,Katalenic, Darinka,Skaric, Djurdjica,Salaj, Ivanka

, p. 2091 - 2098 (2007/10/02)

The synthesis of 5'-N-(N-t-butoxycarbonyl-glycyl)-(6), 5'-N-(N-t-butoxycarbonyl-L-phenylalanyl- (7), and 5'-N-(N-benzyloxycarbonyl-L-phenylalanyl)- (8) derivatives of 5'-amino-5'-deoxy-2',3'-O-isopropylidene-5,6-dihydrouridine by the active ester method i

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