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Thietane-3-carboxylic acid is a heterocyclic organic compound characterized by a three-membered ring with one sulfur and two carbon atoms, featuring a carboxylic acid group attached to the ring. It is recognized for its potential as an anticonvulsant and its unique structural properties, which make it a valuable building block in the synthesis of pharmaceuticals and agrochemicals. Its biological activity and therapeutic effects on neurological disorders have garnered significant interest in medicinal chemistry and drug discovery research.

765-55-9

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765-55-9 Usage

Uses

Used in Pharmaceutical Industry:
Thietane-3-carboxylic acid is used as a building block for the synthesis of various pharmaceuticals due to its unique structural properties and biological activity, contributing to the development of novel drug candidates.
Used in Agrochemical Industry:
Thietane-3-carboxylic acid is utilized as a key component in the synthesis of agrochemicals, leveraging its chemical properties to create effective compounds for agricultural applications.
Used in Neurological Disorder Treatment:
Thietane-3-carboxylic acid is employed as a potential anticonvulsant agent for the treatment of neurological disorders, given its demonstrated therapeutic effects and potential to modulate relevant biological pathways.
Used in Drug Discovery Research:
In the field of drug discovery, thietane-3-carboxylic acid serves as an important molecule for research, providing insights into the development of new therapeutic agents and enhancing understanding of its role in medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 765-55-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,6 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 765-55:
(5*7)+(4*6)+(3*5)+(2*5)+(1*5)=89
89 % 10 = 9
So 765-55-9 is a valid CAS Registry Number.

765-55-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Thietane-3-carboxylic acid

1.2 Other means of identification

Product number -
Other names thietan-3-carboxylic acid

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:765-55-9 SDS

765-55-9Downstream Products

765-55-9Relevant academic research and scientific papers

TETRAHYDROPYRIDOPYRIMIDINES AND TETRAHYDROPYRIDOPYRIDINES AS INHIBITORS OF HBSAG (HBV SURFACE ANTIGEN) AND HBV DNA PRODUCTION FOR THE TREATMENT OF HEPATITIS B VIRUS INFECTIONS

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Page/Page column 170, (2016/11/21)

The present invention provides tetrahydropyridopyrimidines and tetrahydropyridopyridines having the general formula (I) wherein R1, R2, U, W, X, Y and Z are as described herein, as inhibitors of HBsAg (HBV surface antigen) and HBV DNA production for the treatment and prophylaxis of hepatitis B virus infections.

PROCESSES FOR THE PREPARATION OF THIETANAMINE

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Page/Page column 34, (2013/03/26)

The present invention provides processes for the preparation of compounds of formula (I) including processes comprising a. reacting a compound of formula (II) with a nucleophile in the presence of water to give a compound comprising a thietane moiety in which the carbon atom at the 3 position of the thietane moiety is bonded to a nitrogen atom; wherein the nucleophile is selected the group consisting of: N3-, a sulfonamide having two hydrogen atoms bound to the nitrogen atom, a diimide having a hydrogen atom bound to the nitrogen atom or an anion thereof, NH2OH and NH3; and b. when the nucleophile used in step a. is N3- or NH2OH, reacting the compound produced in step a. with a suitable reducing agent to give a compound of formula (I); or when the nucleophile used in step a. is a sulfonamide, reacting the compound produced in step a. with a reagent suitable for cleaving the S-N bond of the sulfonamide group to give a compound of formula (I); or when the nucleophile used in step a. is a diimide, reacting the compound produced in step a. with a reagent suitable for cleaving the C-N bond of the amide group to give a compound of formula (I). The invention also relates to intermediates useful for the preparation of compounds of formula (I).

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