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[1,2,4]Triazolo[1,5-a]pyrimidine, 5,7-dimethyl-2-[(phenylmethyl)thio]- is a complex organic compound with the chemical formula C15H14N4S. It belongs to the class of triazolo[1,5-a]pyrimidines, which are heterocyclic compounds with a triazole ring fused to a pyrimidine ring. This specific compound features two methyl groups at the 5 and 7 positions, a phenylmethylthio group at the 2 position, and a sulfur atom in the thiol functional group. It is likely to be used in pharmaceutical or chemical research due to its unique structure and potential biological activity.

51646-15-2

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51646-15-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51646-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,6,4 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51646-15:
(7*5)+(6*1)+(5*6)+(4*4)+(3*6)+(2*1)+(1*5)=112
112 % 10 = 2
So 51646-15-2 is a valid CAS Registry Number.

51646-15-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzylsulfanyl-5,7-dimethyl-[1,2,4]triazolo[1,5-a]pyrimidine

1.2 Other means of identification

Product number -
Other names HMS2785N04

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:51646-15-2 SDS

51646-15-2Relevant academic research and scientific papers

On triazoles. XXXV. The reaction of 5-amino-1,2,4-triazoles with di- and triketones

Reiter,Pongo,Kovesdi,Pallagi

, p. 407 - 417 (2007/10/02)

The reaction of 5-amino-3-Q-1H-1,2,4-triazoles 1 with aliphatic, aromatic and cyclic 1,3-diketones, 1,4-diketones, and different linear and non linear triketones was studied. It was proved that in case of unsymmetrical aliphatic 1,3-diketones the regiochemical outcome of the reaction was influenced by steric factors. In case of triacetylmethane and 3-(4-chlorobenzyl)-2,4-pontanedione the splitting of one acetyl group from the reactant was observed during the reaction. A liner triketone, namely the 2,4,6-trioxoheptane reacted as a simple 1,3-diketone.

Substituted 1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamides, compositions containing them, and their utility as herbicides

-

, (2008/06/13)

Novel substituted triazolo[1,5-a]pyrimidine-2-sulfonamides, e.g., 5,7-dimethyl-N-(2,6-dichlorophenyl)-1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamide and their agriculturally acceptable salts are prepared. These compounds and compositions containing them are useful for the control of unwanted vegetation. Novel substituted triazolo[1,5-a]pyrimidine-2-sulfonyl chlorides and substituted anilines and their use as intermediates are also described.

Novel substituted 1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamides and compositions and method for inhibiting pollen formation in corn

-

, (2008/06/13)

Novel compounds, e.g., 5,7-dimethyl-N-(2,6-dichlorolphenyl)-1,2,4-triazolo[1,5-a]pyrimidine-2-sulfonamide and their compositions and use in the control of weeds and in the suppression of nitrification of ammonium nitrogen in soil. Other novel compounds and their compositions and use in the inhibition of bolting in sugar beets. Other novel compounds and their compositions and use as plant gametocides.

2-(Alkylthio)-1,2,4-triazolo[1,5-a]pyrimidines as adenosine cyclic 3',5'-monophosphate phosphodiesterase inhibitors with potential as new cardiovascular agents

Novinson,Springer,O'Brien,Scholten,Miller,Robins

, p. 420 - 426 (2007/10/02)

A series of new 2-(alkylthio)-5,7-disubstituted-1,2,4-triazolo[1,5-a]pyrimidines have been prepared as inhibitors of cAMP phosphodiesterase from various tissues. These derivatives were prepared via ring closure of various requisite 3-amino-1,2,4-triazole

2-SUBSTITUTED-S-TRIAZOLO[1,5A]-PYRIMIDINES

-

, (2008/06/13)

2-Substituted-s-triazolo[1,5a]pyrimidines are disclosed which are useful as inhibitors of phosphodiesterase enzymes or intermediates in the production process. Such comoounds are of the following structure: wherein X, R, R1, R2 and R3 are as defined herei

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