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4,6-Dihydrothieno[3,4-b]thiophene-2-carboxylic acid is an organic compound characterized by a unique heterocyclic structure consisting of thiophene and thiophene-2-carboxylic acid moieties. It is a versatile intermediate in the synthesis of various organic and pharmaceutical compounds due to its chemical reactivity and structural properties.

7712-05-2

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7712-05-2 Usage

Uses

Used in Organic Synthesis:
4,6-Dihydrothieno[3,4-b]thiophene-2-carboxylic acid is used as an organic synthesis intermediate for the preparation of a wide range of chemical compounds. Its unique structure allows for various chemical reactions, such as substitution, addition, and condensation, enabling the synthesis of complex organic molecules with potential applications in different industries.
Used in Pharmaceutical Industry:
4,6-Dihydrothieno[3,4-b]thiophene-2-carboxylic acid is used as a pharmaceutical intermediate in the development of new drugs and therapeutic agents. Its chemical properties make it a valuable building block for the synthesis of pharmaceutical compounds with potential applications in treating various diseases and medical conditions.
Used in Laboratory Research and Development:
4,6-Dihydrothieno[3,4-b]thiophene-2-carboxylic acid is utilized in laboratory research and development processes to explore its chemical properties, reactivity, and potential applications in various fields. Researchers use 4,6-Dihydrothieno[3,4-b]thiophene-2-carboxylic acid to investigate new synthetic routes, reaction mechanisms, and the development of novel chemical compounds with specific properties and functions.
Used in Chemical Production Processes:
4,6-Dihydrothieno[3,4-b]thiophene-2-carboxylic acid is employed in chemical production processes to manufacture a variety of chemical products, including pharmaceuticals, agrochemicals, and specialty chemicals. Its versatility as a synthetic intermediate allows for the efficient production of target compounds with desired properties and applications.

Synthesis

Compound 3 was dissolved in ethanol,Potassium hydroxide was added and refluxed at 78 ° C for 4 h,After cooling to room temperature (25 ° C), the reaction solution was extracted with IM HCl, extracted with ethyl acetate, dried over Mg2SO4 and dried to give the title compound 4 (92%).

Check Digit Verification of cas no

The CAS Registry Mumber 7712-05-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,1 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7712-05:
(6*7)+(5*7)+(4*1)+(3*2)+(2*0)+(1*5)=92
92 % 10 = 2
So 7712-05-2 is a valid CAS Registry Number.

7712-05-2 Well-known Company Product Price

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  • TCI America

  • (D4071)  4,6-Dihydrothieno[3,4-b]thiophene-2-carboxylic Acid  >98.0%(GC)(T)

  • 7712-05-2

  • 1g

  • 3,990.00CNY

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7712-05-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-Dihydrothieno[3,4-<i>b</i>]thiophene-2-carboxylic Acid

1.2 Other means of identification

Product number -
Other names 4,6-Dihydrothieno[3,4-b]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:7712-05-2 SDS

7712-05-2Relevant academic research and scientific papers

Fused-heterocycle compound and preparation method thereof

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Paragraph 0127, (2017/06/23)

The invention discloses a fused-heterocycle compound and a preparation method thereof. A structural general formula is shown as formula 1, X is selected from S or Se; Y is selected from one of S, Se or O; R1 and R2 are selected from hydrogen or iodine, and R1 and R2 are different; R3 is selected from any one of -OH, -OR4 or a polyether group, wherein R4 is an alkyl of a straight chain or a branched chain of C1-C30 or an alkyl of a straight chain or a branched chain of C1-C30 which is substituted by halogen. A series of reactions and hydrolysis are carried out in order to obtain the compound, and at the same time, an intermediate shown in a formula 2 and a preparation method thereof are provided. The preparation method is simple, raw materials have wide sources, products of each reaction have high yields, and obtained yields of target products are higher; the compound shown in the formula 1 can be applied to synthesis of a semi-conducting polymer, and can be used as parent compounds for synthesis of other fused-heterocycle compounds. Structural modification can be carried out in a plurality of modes for the middle shown in the formula 2, so that derivatives with a plurality of structures are obtained.

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