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2,3-dihydrocyclopenta[b]thiochromen-9(1H)-one is a heterocyclic organic compound characterized by a five-membered ring structure with a sulfur atom and a carbonyl group. 2,3-dihydrocyclopenta[b]thiochromen-9(1H)-one is a derivative of cyclopenta[b]thiochromene, which is a type of thiochromene, a class of compounds that contain a thiophene ring fused to a chromene ring. The 2,3-dihydro prefix indicates that the compound has two hydrogen atoms added across the double bond between the second and third carbon atoms, making it a dihydro derivative. The 9(1H)-one suffix specifies the position of the carbonyl group (at the ninth position) and the presence of a hydrogen atom attached to it, indicating an enolic form. 2,3-dihydrocyclopenta[b]thiochromen-9(1H)-one may have potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity.

4734-86-5

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4734-86-5 Usage

Structure

Cyclic with sulfur, carbon, and oxygen atoms
The compound has a ring-like structure containing these three types of atoms.

Heterocyclic compound

Yes
The compound contains at least one atom that is not carbon (e.g., sulfur) within its ring structure.

Family

Thiochromen
It belongs to the thiochromen family of compounds, which are known for their diverse chemical properties.

Usage

Organic synthesis and medicinal chemistry
The compound is commonly used as an intermediate or building block in the synthesis of other compounds in both organic chemistry and the development of pharmaceuticals.

Potential biological activities

Yes
2,3-dihydrocyclopenta[b]thiochromen-9(1H)-one has potential biological activities that make it of interest in the field of medicinal chemistry.

Derivatives

Studied for pharmacological properties
The modified forms of 2,3-dihydrocyclopenta[b]thiochromen-9(1H)-one have been researched for their potential effects on living organisms, particularly as anticancer and antimicrobial agents.

Importance

Versatile building block in pharmaceuticals and agrochemicals
Due to its unique structure and functional groups, the compound serves as an important intermediate in the synthesis of various bioactive compounds, making it valuable in the development of new drugs and agrochemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 4734-86-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,3 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4734-86:
(6*4)+(5*7)+(4*3)+(3*4)+(2*8)+(1*6)=105
105 % 10 = 5
So 4734-86-5 is a valid CAS Registry Number.

4734-86-5SDS

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 2,3-dihydro-1H-cyclopenta[b]thiochromen-9-one

1.2 Other means of identification

Product number -
Other names 2,3-Benzo-5,6-cyclopenteno-1-thio-pyron-(4)

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:4734-86-5 SDS

4734-86-5Downstream Products

4734-86-5Relevant academic research and scientific papers

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