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4-Thiazolidinecarboxylic acid, 3-methyl, (R)-(9CI) is a thiazolidine derivative, an organic heterocyclic compound with the molecular formula C5H9NO2S. It features a chiral center, indicated by the (R)-(9CI) designation, and contains both sulfur and nitrogen atoms in its ring structure. 4-Thiazolidinecarboxylicacid,3-methyl-,(R)-(9CI) has been studied for its potential pharmaceutical and bioactive properties, such as anti-inflammatory and anti-tumor activities. The 3-methyl substitution on the thiazolidine ring may further influence its biological activity and chemical reactivity. Further investigation is required to fully understand its detailed chemical and pharmacological properties and potential applications.

60129-40-0

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60129-40-0 Usage

Uses

Used in Pharmaceutical Industry:
4-Thiazolidinecarboxylic acid, 3-methyl, (R)-(9CI) is used as a pharmaceutical intermediate for the development of drugs with potential anti-inflammatory and anti-tumor activities. Its unique structure and chiral center may contribute to its biological activity and selectivity, making it a promising candidate for drug discovery and optimization.
Used in Bioactive Compound Research:
4-Thiazolidinecarboxylic acid, 3-methyl, (R)-(9CI) is used as a bioactive compound in research studies to explore its potential therapeutic effects and mechanisms of action. Its anti-inflammatory and anti-tumor properties may provide insights into the development of novel treatments for various diseases and conditions.
Used in Chemical Synthesis:
4-Thiazolidinecarboxylic acid, 3-methyl, (R)-(9CI) can be used as a building block or precursor in the synthesis of other complex organic compounds, including pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity may enable the development of new synthetic routes and methodologies.
Used in Analytical Chemistry:
4-Thiazolidinecarboxylic acid, 3-methyl, (R)-(9CI) can be employed as a chiral reference standard or analytical reagent in various chromatographic and spectroscopic techniques. Its enantiomeric forms can be used to study enantioselectivity, chiral recognition, and stereochemistry in chemical and biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 60129-40-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,2 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 60129-40:
(7*6)+(6*0)+(5*1)+(4*2)+(3*9)+(2*4)+(1*0)=90
90 % 10 = 0
So 60129-40-0 is a valid CAS Registry Number.

60129-40-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-1,3-thiazolidine-4-carboxylic acid,hydrochloride

1.2 Other means of identification

Product number -
Other names 4-Thiazolidinecarboxylic acid,3-methyl-,hydrochloride

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:60129-40-0 SDS

60129-40-0Downstream Products

60129-40-0Relevant academic research and scientific papers

An Efficient, One-Pot Synthesis of 3-Methyl-1,3-thiazolidines

Ando, Wataru,Takata, Toshikazu,Huang, Liren,Tamura, Yoshiharu

, p. 139 - 140 (2007/10/02)

3-Methyl 1,3-thiazolidines 3a-c can be prepared easily in good yields by the reaction of β-mercaptoamine derivatives 1a-c with formalin and formic acid in a one-pot operation.The same procedure is also suitable for the construction of the 3-methyl-tetrahydro-1,3-thiazine skeleton from γ-mercaptoamines as exemplified in the synthesis of 3d.

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