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N~3~,N~3~-dimethyl-1H-1,2,4-triazole-3,5-diamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51108-33-9

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51108-33-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51108-33-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,0 and 8 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51108-33:
(7*5)+(6*1)+(5*1)+(4*0)+(3*8)+(2*3)+(1*3)=79
79 % 10 = 9
So 51108-33-9 is a valid CAS Registry Number.

51108-33-9SDS

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 3-N,3-N-dimethyl-1H-1,2,4-triazole-3,5-diamine

1.2 Other means of identification

Product number -
Other names 1H-1,4-Triazole-3,5-diamine,N,N-dimethyl

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:51108-33-9 SDS

51108-33-9Relevant articles and documents

On Triazoles. XXVIII. Synthesis of Isomeric 1,2,4-Triazolylcarbothiohydrazides

Barkoczy, Jozsef,Reiter, Jozsef

, p. 1677 - 1683 (2007/10/02)

Different 3a, 3b, 9, 10 and 12 type 5-amino-1,2,4-triazolylcarbothiohydrazide isomers representing all possible isomeric types derived from 5-amino-1,2,4-triazoles were synthesised from the corresponding 5-amino-1,2,4-triazolyldithiocarbonates and hydrazines.HPLC measurements proved that in case of monosubstituted hydrazines the steric press in the intermediate 6 caused besides formation of the expected derivative 3a the formation of compounds 4 and 5, too, while the intermediate 7 yielded only 3b.Thermal rearangement of derivatives 3a in acetic acid led to isomers 9 and 10, respectively.

On Triazoles. V . Synthesis of 1- and 2-R1-3-R2,R3-Amino-5-amino-1,2,4-triazoles

Reiter, Jozsef,Pongo, Laszlo,Somorai, Tamas,Dvortsak, Peter

, p. 401 - 408 (2007/10/02)

The correct isomeric and tautomeric structure of different 1- and 2-R1-3-R2,R3-amino-5-amino-1,2,4-triazole derivatives prepared from the corresponding N-cyano-N'-R2,R3-S-methyl-isothioureas and the corresponding hydrazines was proved with the help of their ir, uv, 1H-nmr and 13C-nmr spectra as well as the uv spectra of the Schiff bases of an isomeric pair.

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