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219582-35-1

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219582-35-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 219582-35-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,5,8 and 2 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 219582-35:
(8*2)+(7*1)+(6*9)+(5*5)+(4*8)+(3*2)+(2*3)+(1*5)=151
151 % 10 = 1
So 219582-35-1 is a valid CAS Registry Number.

219582-35-1SDS

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-{1,2-dihydro-2-oxo-1-[tetrahydro-4-hydroxy-5-(hydroxymethyl)furan-2-yl]pyrimidin-4-yl}-N'-phenylurea

1.2 Other means of identification

Product number -
Other names 2'-deoxy-N4-[(phenylamino)carbonyl]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:219582-35-1 SDS

219582-35-1Relevant articles and documents

Nucleotides: Part LXXV. New types of fluorescence labeling of 2′-deoxycytidine

Maier, Thomas,Pfleiderer, Wolfgang

experimental part, p. 2722 - 2736 (2010/04/04)

The reactivity of the 2′-deoxy-N4-(phenoxycarbonyl) cytidine derivatives 3 and 4 with aromatic amines was studied to form new types of urea derivatives (see 5 - 10). On the same basis, labeling of 3 and 4 with 5-aminofluorescein (14) was achiev

Synthesis and hybridization affinity of oligodeoxyribonucleotides incorporating 4-N-(N-arylcarbamoyl)deoxycytidine derivatives

Miyata, Kenichi,Tamamushi, Ryuji,Ohkubo, Akihiro,Taguchi, Haruhiko,Seio, Kohji,Sekine, Mitsuo

, p. 9365 - 9368 (2007/10/03)

Modified oligodeoxynucleotides incorporating 4-N-(N-arylcarbamoyl)-dC derivatives 1a-c were synthesized. The 1H NMR spectra of 1a-c suggest that the carbamoyl group forms an intramolecular hydrogen bond with the cytosine ring nitrogen atom so t

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