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14305-99-8

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14305-99-8 Usage

Derivative of

Barbituric acid

Usage

Intermediate in the synthesis of pharmaceuticals and other organic compounds

Appearance

Yellow crystalline

Potential hazard

Explosive under certain conditions

Safety concerns

Requires careful handling and storage to avoid safety risks

Field of significance

Organic chemistry

Industrial applications

Various, including pharmaceutical synthesis

Check Digit Verification of cas no

The CAS Registry Mumber 14305-99-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,3,0 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14305-99:
(7*1)+(6*4)+(5*3)+(4*0)+(3*5)+(2*9)+(1*9)=88
88 % 10 = 8
So 14305-99-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H7N3O5/c1-7-4(10)3(9(13)14)5(11)8(2)6(7)12/h3H,1-2H3

14305-99-8SDS

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 1,3-dimethyl-5-nitro-1,3-diazinane-2,4,6-trione

1.2 Other means of identification

Product number -
Other names 1,3-dimethyl-5-nitro-2,4,6-pyrimidinetrione

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:14305-99-8 SDS

14305-99-8Downstream Products

14305-99-8Relevant articles and documents

Concerning the reaction of 4-chlor-5-nitro-pyrimidines with glucosamine

Pfleiderer,Bühler,Schmidt

, p. 3794 - 3801 (1968)

-

Nitration of 2-substituted pyrimidine-4,6-diones, structure and reactivity of 5,5-gem-dinitropyrimidine-4,6-diones

Langlet, Abraham,Latypov, Nikolaj V.,Wellmar, Ulf,Bemm, Ulf,Goede, Patrick,Bergman, Jan,Romero, Ivan

, p. 7833 - 7838 (2007/10/03)

Nitration of some 2-substituted pyrimidine-4,6-diones in sulfuric acid was studied, which afforded previously unknown 5,5-gem-dinitropyrimidine-4,6-diones in high yields. The gem-dinitro products were easily attacked by nucleophiles with concomitant formation of gem-dinitroacetyl derivatives, which in turn could be further hydrolyzed to salts of dinitromethane and triureas.

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