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2-(2,6-dichlorophenyl)-3-pyrazin-2-yl-1,3-thiazolidin-4-one is a complex organic compound with the molecular formula C12H7Cl2N3OS. It is characterized by a 1,3-thiazolidin-4-one core, which is a five-membered heterocyclic ring containing sulfur and oxygen. The molecule features a 2,6-dichlorophenyl group attached to the 2-position of the thiazolidinone ring, and a pyrazin-2-yl group at the 3-position. This chemical structure is significant in the field of medicinal chemistry, as it is the active ingredient in a class of drugs used to treat type 2 diabetes. The compound works by inhibiting the enzyme dipeptidyl peptidase-4 (DPP-4), which plays a role in the regulation of blood glucose levels. By blocking DPP-4, the compound helps to increase the levels of insulin-releasing hormones, thereby improving glycemic control. This class of drugs is known for their oral administration and their role in managing postprandial hyperglycemia, making them a valuable tool in the treatment of diabetes.

96733-49-2

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96733-49-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96733-49-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,7,3 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 96733-49:
(7*9)+(6*6)+(5*7)+(4*3)+(3*3)+(2*4)+(1*9)=172
172 % 10 = 2
So 96733-49-2 is a valid CAS Registry Number.

96733-49-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2,6-dichlorophenyl)-3-pyrazin-2-yl-1,3-thiazolidin-4-one

1.2 Other means of identification

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Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

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More Details:96733-49-2 SDS

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