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59025-32-0

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59025-32-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59025-32-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,0,2 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59025-32:
(7*5)+(6*9)+(5*0)+(4*2)+(3*5)+(2*3)+(1*2)=120
120 % 10 = 0
So 59025-32-0 is a valid CAS Registry Number.

59025-32-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(aminomethylidene)-1,3-diazinane-2,4,6-trione

1.2 Other means of identification

Product number -
Other names 5-Aminomethylen-barbitursaeure

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:59025-32-0 SDS

59025-32-0Relevant articles and documents

Azoles and azines. XCIX. some reactions of oxo derivatives of 5,5′-ylidenedipyrimidines and 5H-pyrano[2,3-d:6,5-d′]dipyrimidines

Moskvin,Petrova,Krasnov,Ivin

, p. 803 - 810 (2007/10/03)

5,5′-Alkylidene(arylmethylene)dipirimidin-4,4′,6,6′- tetraols and 5-alkyl(aryl)-5H-pyrano-[2,3-d:6,5-d′]dipyrimidine-4,6(3H,7H)-diones react with POCl3, yielding mainly 4,6-dichloro-5H-pyrano-[2,3-d:6,5-d′]dipyrimidines. The chlorine atoms in the latter compounds are readily replaced by the action of nucleophiles, such as sodium methoxide and benzylamine. Hydrogen sulfite ion adds at C2 of 5,5′-alkylidene-(arylmethylene)dipyrimidine-4,4′,6,6′- tetraols. Barbituric acid also attacks position 2 of the pyrimidine ring, resulting in decomposition of the substrate to give 5-aminomethylenebarbituric acid or its derivatives. Alkylation of 5-alkyl(aryl)-5H-pyrano[2,3-d:6,5-d′]dipyrimidine-4,6(3H,7H)-diones with dimethyl sulfate and methyl iodide occurs at the nitrogen atoms, whereas diazomethane reacts at both nitrogen and oxygen atoms.

SYNTHESIS OF 2,2-BIS(ARYLSULFONYL)VINYLAMINES, THEIR ANALOGS, AND SYMMETRICAL TRIMETHINECYANINES BY MEANS OF BIS(TRIMETHYLSILYL)FORMAMIDE

Lazukina, L. A.,Mushkalo, I. L.,Neplyuev, V. M.,Kukhar', V. P.

, p. 2114 - 2117 (2007/10/02)

The reactions of compounds containing active methylene and methyl groups (β-disulfones, arylsulfonylacetonitriles, barbituric acid, rhodanines, methylsubstituted quaternary salts of nitrogen heterocycles) with bis(trimethylsilyl)formamide were investigate

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