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4-Methyl-3-amino-2-(methoxycarbonyl)-4,5-dihydrothiophene is a chemical compound that features a unique combination of functional groups. Its molecular structure comprises a thiophene ring, a heterocyclic compound that contains sulfur, which is bonded to a methyl group, an amino group, and a methoxycarbonyl group. The properties, reactivity, and behavior of 4-METHYL-3-AMINO-2-(METHOXYCARBONYL)-4,5-DIHYDROTHIOPHENE are determined by the interactions of these groups. Despite its potential applications, detailed information about its physical properties, uses, production methods, toxicity, or health effects is not extensively documented in scientific literature, indicating its specialized and niche nature within the field of chemistry.

125089-02-3

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125089-02-3 Usage

Uses

Due to the limited information available, the specific applications of 4-Methyl-3-amino-2-(methoxycarbonyl)-4,5-dihydrothiophene are not well-defined. However, based on the functional groups present in its structure, it can be inferred that 4-METHYL-3-AMINO-2-(METHOXYCARBONYL)-4,5-DIHYDROTHIOPHENE may have potential uses in various industries, such as:
Used in Pharmaceutical Industry:
4-Methyl-3-amino-2-(methoxycarbonyl)-4,5-dihydrothiophene could be used as an intermediate or building block in the synthesis of pharmaceutical compounds. The presence of the thiophene ring, amino, and methoxycarbonyl groups may allow for the development of new drugs with unique properties and therapeutic effects.
Used in Chemical Synthesis:
In the field of organic chemistry, 4-Methyl-3-amino-2-(methoxycarbonyl)-4,5-dihydrothiophene may serve as a starting material or intermediate in the synthesis of more complex molecules. Its functional groups could be utilized in various chemical reactions, leading to the formation of new compounds with potential applications in different industries.
Used in Material Science:
4-METHYL-3-AMINO-2-(METHOXYCARBONYL)-4,5-DIHYDROTHIOPHENE's structure may also lend itself to applications in material science, where it could be used as a component in the development of new materials with specific properties. The thiophene ring, in particular, is known to be a key structural element in many conductive polymers and organic semiconductors, suggesting potential uses in electronic devices or sensors.

Check Digit Verification of cas no

The CAS Registry Mumber 125089-02-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,0,8 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 125089-02:
(8*1)+(7*2)+(6*5)+(5*0)+(4*8)+(3*9)+(2*0)+(1*2)=113
113 % 10 = 3
So 125089-02-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H11NO2S/c1-4-3-11-6(5(4)8)7(9)10-2/h4H,3,8H2,1-2H3

125089-02-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 4-amino-3-methyl-2,3-dihydrothiophene-5-carboxylate

1.2 Other means of identification

Product number -
Other names 3-amino-2-carbomethoxy-4-methyl-4,5-dihydrothiophene

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:125089-02-3 SDS

125089-02-3Relevant academic research and scientific papers

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