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5390-61-4

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5390-61-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5390-61-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,9 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5390-61:
(6*5)+(5*3)+(4*9)+(3*0)+(2*6)+(1*1)=94
94 % 10 = 4
So 5390-61-4 is a valid CAS Registry Number.
InChI:InChI=1/C3H7Cl2PS2/c1-2-3-8-6(4,5)7/h2-3H2,1H3

5390-61-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-diamino-1,4-dihydropyrimidine-5,6-dione

1.2 Other means of identification

Product number -
Other names 2,5-Diamino-4,5-diketopyrimidine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates
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:5390-61-4 SDS

5390-61-4Relevant articles and documents

Exchange reactions of tetrathiophosphates with thiophosphoryl chloride

Khokhlov,Sokolova,Osipov,Savenkov

, p. 1768 - 1770 (2007/10/03)

Exchange reactions of tetrathiophosphates with thiophosphoryl chloride were studied. The exchange of thiol groups between compounds with tetracoordinated phosphorus centers proceeds at 150-220 °C and results in the formation of dialkyl trithiochlorophosphates and alkyl(aryl) dithiodichlorophosphates or their mixtures depending on the ratio of the reagents.

Process for preparing phosphorodichloridodithioates by reacting alkyl mercaptans with PCI3 PSCI3 and sulfur

-

, (2008/06/13)

Disclosed herein is a process for preparing a phosphorodichloridodithioate comprising reacting a mercaptan, phosphorus trichloride, thiophosphoryl chloride and sulfur in the presence of a base catalyst.

Process for preparing mono- and disubstituted mercapto-phosphorothionochloridates

-

, (2008/06/13)

Mono- and disubstituted mercaptophosphorothionochloridates are prepared by reacting a disubstituted sulfide having the formula wherein each R is an independently selected alkyl, cycloalkyl or benzyl, with phosphorus pentasulfide and thiophosphorus trichloride at a temperature from about 150° to about 300° C. A molar ratio of R2 S to P4 S10 to P(S)Cl3 of 6:1:8 is preferred where the monosubstituted compound is desired, while a ratio of 6:1:2 is preferred where the disubstituted compound is desired. The compounds are useful as intermediates for compounds which exhibit biocidal properties, particularly insecticides and herbicides.

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