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1,2,4-Triazolo[4,3-a]pyrazine, 5,6,7,8-tetrahydro-5,5-dimethyl-3-(trifluoromethyl)is a heterocyclic chemical compound characterized by the presence of a triazolopyrazine ring and a trifluoromethyl group. 1,2,4-Triazolo[4,3-a]pyrazine, 5,6,7,8-tetrahydro-5,5-dimethyl-3-(trifluoromethyl)holds potential in various fields such as pharmaceuticals, agrochemicals, and materials science due to its unique molecular structure and properties.

723286-97-3

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723286-97-3 Usage

Uses

Used in Pharmaceutical Industry:
1,2,4-Triazolo[4,3-a]pyrazine, 5,6,7,8-tetrahydro-5,5-dimethyl-3-(trifluoromethyl)is used as a building block for the development of new drugs. The trifluoromethyl group enhances the metabolic stability of drug molecules, which can improve their pharmacokinetic properties and therapeutic efficacy.
Used in Agrochemical Industry:
In the agrochemical field, 1,2,4-Triazolo[4,3-a]pyrazine, 5,6,7,8-tetrahydro-5,5-dimethyl-3-(trifluoromethyl)may be utilized as a key intermediate in the synthesis of novel agrochemicals with improved performance and selectivity.
Used in Materials Science:
1,2,4-Triazolo[4,3-a]pyrazine, 5,6,7,8-tetrahydro-5,5-dimethyl-3-(trifluoromethyl)has potential applications in the development of new materials due to its unique chemical and physical properties. Its heterocyclic structure and trifluoromethyl group may contribute to the creation of materials with enhanced properties for various applications.
Further research and development of 1,2,4-Triazolo[4,3-a]pyrazine, 5,6,7,8-tetrahydro-5,5-dimethyl-3-(trifluoromethyl)- may lead to the discovery of new drugs, agrochemicals, or materials with valuable properties, expanding its applications across different industries.

Check Digit Verification of cas no

The CAS Registry Mumber 723286-97-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,3,2,8 and 6 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 723286-97:
(8*7)+(7*2)+(6*3)+(5*2)+(4*8)+(3*6)+(2*9)+(1*7)=173
173 % 10 = 3
So 723286-97-3 is a valid CAS Registry Number.

723286-97-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5,5-dimethyl-3-(trifluoromethyl)-7,8-dihydro-6H-[1,2,4]triazolo[4,3-a]pyrazine

1.2 Other means of identification

Product number -
Other names 1,2,4-Triazolo[4,3-a]pyrazine,5,6,7,8-tetrahydro-5,5-dimethyl-3-(trifluoromethyl)

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:723286-97-3 SDS

723286-97-3Downstream Products

723286-97-3Relevant academic research and scientific papers

Discovery of potent and selective dipeptidyl peptidase IV inhibitors derived from β-aminoamides bearing subsituted triazolopiperazines

Kim, Dooseop,Kowalchick, Jennifer E.,Brockunier, Linda L.,Parmee, Emma R.,Eiermann, George J.,Fisher, Michael H.,He, Huaibing,Leiting, Barbara,Lyons, Kathryn,Scapin, Giovanna,Patel, Sangita B.,Petrov, Aleksandr,Pryor, Kelly Ann D.,Roy, Ranabir Sinha,Wu, Joseph K.,Zhang, Xiaoping,Wyvratt, Matthew J.,Zhang, Bei B.,Zhu, Lan,Thornberry, Nancy A.,Weber, Ann E.

, p. 589 - 602 (2008/09/17)

A series of β-aminoamides bearing triazolopiperazines have been discovered as potent, selective, and orally active dipeptidyl peptidase IV (DPP-4) inhibitors by extensive structure-activity relationship (SAR) studies around the triazolopiperazine moiety.

3-AMINO-4-PHENYLBUTANOIC ACID DERIVATIVES AS DIPEPTIDYL PEPTIDASE INHIBITORS FOR THE TREATMENT OR PREVENTION OF DIABETES

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Page/Page column 89, (2010/02/07)

The present invention is directed to 3-amino-4-phenylbutanoic acid derivatives which are inhibitors of the dipeptidyl peptidase-IV enzyme ("DP-IV inhibitors") and which are useful in the treatment or prevention of diseases in which the dipeptidyl peptidase-IV enzyme is involved, such as diabetes and particularly type 2 diabetes. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which the dipeptidyl peptidase-IV enzyme is involved.

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