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4,5-Dihydronaphtho[1,2-b]thiophene-2-carboxylic acid is an organic compound with a complex multi-ringed structure that includes a thiophene ring and a carboxylic acid group. Its synthesis is likely targeted for specific applications in research or industry, potentially as a pharmaceutical intermediate, polymer additive, or specialty chemical in advanced materials. The presence of the thiophene ring may provide unique reactivity or properties, as thiophene derivatives are common in drugs and bioactive compounds. The carboxylic acid group offers a point for further chemical modification, enabling the creation of a variety of potential derivatives.

29179-41-7

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29179-41-7 Usage

Uses

Used in Pharmaceutical Industry:
4,5-Dihydronaphtho[1,2-b]thiophene-2-carboxylic acid is used as a pharmaceutical intermediate for its potential to be incorporated into drug molecules. The thiophene ring may contribute to the drug's bioactivity, while the carboxylic acid group allows for further chemical modifications to optimize the drug's properties.
Used in Polymer Industry:
In the polymer industry, 4,5-Dihydronaphtho[1,2-b]thiophene-2-carboxylic acid is used as a polymer additive to enhance the properties of polymers. The unique reactivity of the thiophene ring may improve the polymer's stability, flexibility, or other characteristics, making it suitable for specific applications.
Used in Advanced Materials:
4,5-Dihydronaphtho[1,2-b]thiophene-2-carboxylic acid is used in the development of advanced materials, where its complex structure and potential reactivity may be harnessed to create materials with novel properties. The carboxylic acid group provides a point for further modification, allowing for the customization of the material's characteristics for specific uses.

Check Digit Verification of cas no

The CAS Registry Mumber 29179-41-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,1,7 and 9 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 29179-41:
(7*2)+(6*9)+(5*1)+(4*7)+(3*9)+(2*4)+(1*1)=137
137 % 10 = 7
So 29179-41-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H10O2S/c14-13(15)11-7-9-6-5-8-3-1-2-4-10(8)12(9)16-11/h1-4,7H,5-6H2,(H,14,15)/p-1

29179-41-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,5-DIHYDRONAPHTHO[1,2-B]THIOPHENE-2-CARBOXYLIC ACID

1.2 Other means of identification

Product number -
Other names 4.5-Dihydronaphtho<1.2-b>thiophen-2-carbonsaeure

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:29179-41-7 SDS

29179-41-7Downstream Products

29179-41-7Relevant academic research and scientific papers

Tricyclic heteroaromatic system amide derivative as well as preparation and application thereof

-

, (2018/11/22)

The invention discloses a tricyclic heteroaromatic system amide derivative. The general formula is as shown in a formula (I), wherein the definitions of R, W1, W2, W3 and W4 are as shown in the specification for details. In addition, the invention also discloses a preparation method and a medicinal composition of the compound. The compound which the invention relates to has high alpha7 receptor binding activity, high selectivity and medium-high-level excitement effect. (The formula is as shown in the description).

4H-Thieno[3,2-c]chromene based inhibitors of Notum Pectinacetylesterase

Han, Qiang,Pabba, Praveen K.,Barbosa, Joseph,Mabon, Ross,Healy, Jason P.,Gardyan, Michael W.,Terranova, Kristen M.,Brommage, Robert,Thompson, Andrea Y.,Schmidt, James M.,Wilson, Alan G.E.,Xu, Xiaolian,Tarver, James E.,Carson, Kenneth G.

, p. 1184 - 1187 (2016/02/23)

A group of small molecule thienochromenes inhibitors of Notum Pectinacetylesterase are described. We developed SAR on three series based on carbon, oxygen and sulfur replacement of the 5-position. In each series, highly potent Notum Pectinacetylesterase inhibitors were identified.

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