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(3-[4-(TRIFLUOROMETHYL)PHENYL]-1,2,4-THIADIAZOL-5-YL)METHANOL is a thiadiazole derivative featuring a trifluoromethylphenyl group at the 3-position of the thiadiazole ring and a methanol group attached to the ring. This chemical compound holds potential pharmaceutical applications due to the trifluoromethyl group's ability to enhance biological activity and pharmacokinetic properties, making it a promising candidate for the development of new drugs.
Used in Pharmaceutical Industry:
(3-[4-(TRIFLUOROMETHYL)PHENYL]-1,2,4-THIADIAZOL-5-YL)METHANOL is used as an active pharmaceutical ingredient for the development of new drugs, leveraging its enhanced biological activity and pharmacokinetic properties to address various therapeutic needs.

851224-81-2

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  • 1,2,4-Thiadiazole-5-methanol, 3-[4-(trifluoromethyl)phenyl]-

    Cas No: 851224-81-2

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851224-81-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 851224-81-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,2,2 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 851224-81:
(8*8)+(7*5)+(6*1)+(5*2)+(4*2)+(3*4)+(2*8)+(1*1)=152
152 % 10 = 2
So 851224-81-2 is a valid CAS Registry Number.

851224-81-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-[4-(trifluoromethyl)phenyl]-1,2,4-thiadiazol-5-yl]methanol

1.2 Other means of identification

Product number -
Other names [3-(4-Trifluoromethyl-phenyl)-[1,2,4]thiadiazol-5-yl]-methanol

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:851224-81-2 SDS

851224-81-2Relevant articles and documents

Synthesis and identification of [1,2,4]thiadiazole derivatives as a new series of potent and orally active dual agonists of peroxisome proliferator-activated receptors α and δ

Shen, Lan,Zhang, Yan,Wang, Aihua,Sieber-McMaster, Ellen,Chen, Xiaoli,Pelton, Patricia,Xu, Jun Z.,Yang, Maria,Zhu, Peifang,Zhou, Lubing,Reuman, Michael,Hu, Zhiyong,Russell, Ronald,Gibbs, Alan C.,Ross, Hamish,Demarest, Keith,Murray, William V.,Kuo, Gee-Hong

, p. 3954 - 3963 (2008/02/11)

Cardiovascular disease is the most common cause of morbidity and mortality in developed nations. To effectively target dyslipidemia to reduce the risk of cardiovascular disease, it may be beneficial to activate the peroxisome proliferator-activated recept

Synthesis of a 5-((Aryloxy)methyl)-3-(4-(trifluoromethyl)phenyl)[1,2,4] thiadiazole derivative: A promising PPARα,δ agonist

Reuman, Michael,Hu, Zhiyong,Kuo, Gee-Hong,Li, Xun,Russell, Ronald K.,Shen, Lan,Youells, Scott,Zhang, Yongzheng

, p. 1010 - 1014 (2012/12/30)

The preparation of the PPARα,δ agonist 2-methyl-2-(2-methyl-4- (3-(4-(trifluoromethyl)phenyl)[1,2,4]thiadiazol-5-ylmethoxy)phenoxy)propionic acid sodium salt (17) is described and compared with earlier in-house preparations of this important target compound. Key concerns around a large-scale synthesis of this thiadiazole derivative were a large number of purification steps, the use of dichlorobenzene as a solvent, and a possible large-scale Baeyer-Villiger oxidation. This paper describes a straightforward preparation of the target agonist using methylhydroquinone (MHQ) as an inexpensive precursor that eliminates the need of an oxidation step.

BENZOAZEPIN-OXY-ACETIC ACID DERIVATIVES AS PPAR-DELTA AGONISTS USED FOR THE INCREASE OF HDL-C, LOWER LDL-C AND LOWER CHOLESTEROL

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Page/Page column 25-26, (2008/06/13)

The invention is directed to compounds of Formula (I) useful as PPAR agonists. Pharmaceutical compositions and methods of treating one or more conditions including, but not limited to, diabetes, nephropathy, neuropathy, retinopathy, polycystic ovary syndr

4-((Phenoxyalkyl)thio)-phenoxyacetic acids and analogs

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Page/Page column 16, (2008/06/13)

The invention features 4-((phenoxyalkyl)thio)-phenoxyacetic acids and analogs, compositions containing them, and methods of using them as PPAR modulators to treat or inhibit the progression of, for example, dyslipidemia.

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