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50610-49-6

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50610-49-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50610-49-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,1 and 0 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 50610-49:
(7*5)+(6*0)+(5*6)+(4*1)+(3*0)+(2*4)+(1*9)=86
86 % 10 = 6
So 50610-49-6 is a valid CAS Registry Number.

50610-49-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,5-dichloro-6-hydroxy-6-methyl-5,6-dihydrouracil

1.2 Other means of identification

Product number -
Other names 5,5-dichloro-6-hydroxy-6-methyl-dihydro-pyrimidine-2,4-dione

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:50610-49-6 SDS

50610-49-6Upstream product

50610-49-6Relevant articles and documents

Oxidative halogenation of 6-methyluracil

Kasradze,Ignatyeva,Khusnutdinov,Suponitskii, K. Yu.,Antipin, M. Yu.,Yunusov

, p. 1018 - 1027 (2013/03/13)

An efficient method has been developed for the preparation of halo derivatives of 6-methyluracil by employing oxidative halogenation. Elemental halogens and potassium halides were used as the halogenating agents, while NaNO3 and H2O2 were used as the oxidizing agents. Iodination of 6-methyl-uracil leads to 5-iodo-6-methyluracil as the single reaction product, while bromination or chlorination lead to 5-halo-6-methyluracil, 5,5-dihalo-6-hydroxy-6-methyl-5,6-dihydrouracil, or their mixture depending on the acidity of the medium and the ratio of the substrate and reagents. Bromination of 5-chloro-6-methyluracil leads to 5-bromo-5-chloro-6-hydroxy-6-methyl-5,6-dihydrouracil, while chlorination of 6-methyl-, 5-bromo-6-methyl-, and 5-chloro-6-methyluracils using gaseous chlorine yields 5,5-dichloro-6-hydroxy-6-methyl-5,6-dihydrouracil.

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