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5--2-thiophenecarboxylic acid is a complex organic chemical compound characterized by the presence of a thiophene ring and multiple functional groups, including a carboxylic acid and N-methylamino groups, along with a protective tert-butoxycarbonyl (Boc) group. This structure suggests potential applications in organic synthesis, particularly for the development of pharmaceuticals and agrochemicals, due to its versatile reactivity and protective Boc functionality.

131052-68-1

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131052-68-1 Usage

Uses

Used in Pharmaceutical Industry:
5--2-thiophenecarboxylic acid is used as a building block or intermediate in the synthesis of various pharmaceutical compounds. Its carboxylic acid group allows for the formation of esters, amides, and other derivatives, which can be crucial for the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 5--2-thiophenecarboxylic acid is utilized as a precursor in the production of crop protection products. Its potential reactivity and the presence of the Boc group can be advantageous for the synthesis of active ingredients with improved efficacy and selectivity in controlling pests and diseases.
Used in Organic Synthesis:
5--2-thiophenecarboxylic acid is employed as a versatile intermediate in organic synthesis, where its functional groups can be selectively modified to yield a variety of target molecules. The Boc group serves as a protecting agent for the amino functionality, which can be selectively removed when needed, allowing for further reactions to take place.
Used in Research and Development:
5--2-thiophenecarboxylic acid is also used in research and development settings to explore its chemical properties and reactivity. Its unique structure can provide insights into new synthetic pathways and the development of novel chemical entities with potential applications in various fields.
Used in Formulation Development:
In the formulation of pharmaceuticals and agrochemicals, 5--2-thiophenecarboxylic acid may be used to improve the solubility, stability, or bioavailability of the final product. Its carboxylic acid group can participate in salt formation or complexation with other molecules, which can be beneficial for the optimization of formulations.

Check Digit Verification of cas no

The CAS Registry Mumber 131052-68-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,0,5 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 131052-68:
(8*1)+(7*3)+(6*1)+(5*0)+(4*5)+(3*2)+(2*6)+(1*8)=81
81 % 10 = 1
So 131052-68-1 is a valid CAS Registry Number.

131052-68-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-[N-(tert-butoxycarbonyl)-N-methylamino]-2-thiophenecarboxylic acid

1.2 Other means of identification

Product number -
Other names 5-(N-tert-butoxycarbonyl-N-methylamino)thiophene-2-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:131052-68-1 SDS

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