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1H-Thieno[3,4-f]isoindole-5,7(3H,6H)-dione, 4,4a,7a,8-tetrahydro-6-phenyl-, 2,2-dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

144498-85-1

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144498-85-1 Usage

Heterocyclic compound

The compound contains a ring structure with at least one sulfur atom in the thieno ring, making it a heterocyclic system.

Thienoisoindole core structure

The central structure of the compound is based on a fusion of thieno and isoindole rings, which contributes to its unique chemical properties.

Cyclic compound

The compound forms a closed ring structure, which is common in many organic compounds and can influence its stability and reactivity.

Sulfur atom presence

The presence of a sulfur atom in the thieno ring can affect the compound's reactivity, polarity, and potential applications in various fields.

Phenyl group

The attachment of a phenyl group (a benzene ring) to the core structure can influence the compound's electronic properties, stability, and potential applications in organic synthesis and materials science.

Dione functional groups

The presence of dione functional groups (two carbonyl groups within the same molecule) can contribute to the compound's reactivity, polarity, and potential uses in pharmaceuticals and materials science.

Tetrahydro

The compound has four hydrogen atoms in its structure, which can affect its stability and reactivity.

Potential applications

Due to its unique structure and functional groups, the compound may have potential applications in organic synthesis, pharmaceuticals, and materials science.

Configuration and functional groups

The specific properties and potential uses of the compound depend on the exact configuration and functional groups attached to the thienoisoindole core.

Further research needed

To fully understand the potential uses and effects of this chemical compound, additional research and analysis are required.

Check Digit Verification of cas no

The CAS Registry Mumber 144498-85-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,4,9 and 8 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 144498-85:
(8*1)+(7*4)+(6*4)+(5*4)+(4*9)+(3*8)+(2*8)+(1*5)=161
161 % 10 = 1
So 144498-85-1 is a valid CAS Registry Number.

144498-85-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-phenylimide of 5,6-dicarboxy-1,3,4,5,6,7-hexahydrobenzo<c>thiophene-2,2-dioxide

1.2 Other means of identification

Product number -
Other names 2,2-Dioxo-6-phenyl-2,3,4,4a,7a,8-hexahydro-1H-2λ6-thieno[3,4-f]isoindole-5,7-dione

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:144498-85-1 SDS

144498-85-1Downstream Products

144498-85-1Relevant academic research and scientific papers

SYNTHESIS OF 3,4-DI(METHYLENE)TETRAHYDROTHIOPHENE-1,1-DIOXIDE AND ITS USE IN ORGANIC SYNTHESIS

Tashbaev, G. A.,Krivchikova, L. Yu.,Nasyrov, I. M.

, p. 139 - 141 (2007/10/02)

A convenient reaction scheme has been developed for obtaining 3,4-di(methylene)tetrahydrothiophene-1,1-dioxide from the readily available 3,4-dimethyl-2,4-dihydrothiophene-1,1-dioxide through 3,4-di(bromomethyl)-2,5-dihydrothiophene-1,1-dioxide.A feasibil

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