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5H-Furo[3,2-g][1]benzopyran-5-one, 2,3,6-triphenyl-9-(phenylacetyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

113769-38-3

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113769-38-3 Usage

Molecular structure

Furobenzopyran core with three phenyl groups attached at positions 2, 3, and 6, and a phenylacetyl group attached at position 9

Potential pharmaceutical or biological activities

Due to its structural features, such as aromatic rings and ketone functional groups

Complexity

Compound with a complex molecular structure

Need for further research

To fully understand its properties and potential applications.

Check Digit Verification of cas no

The CAS Registry Mumber 113769-38-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,7,6 and 9 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 113769-38:
(8*1)+(7*1)+(6*3)+(5*7)+(4*6)+(3*9)+(2*3)+(1*8)=133
133 % 10 = 3
So 113769-38-3 is a valid CAS Registry Number.

113769-38-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,6-triphenyl-9-(2-phenylacetyl)furo[3,2-g]chromen-5-one

1.2 Other means of identification

Product number -
Other names 5H-Furo[3,2-g][1]benzopyran-5-one,2,3,6-triphenyl-9-(phenylacetyl)

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:113769-38-3 SDS

113769-38-3Downstream Products

113769-38-3Relevant academic research and scientific papers

Synthesis of Substituted Furobenzopyrones

Hishmat, O. H.,Rahman, A. H. Abd El,Diwani, H. I. El,Bakr, Sh. M. Abu

, p. 566 - 568 (2007/10/02)

Friedel-Crafts acylation of 2,3-diphenyl-6-methoxybenzofuran (I) using phenylacetyl chloride in CS2 gives a mixture of 5-phenylacetyl (II) and 5,7-diphenylacetyl (III) derivatives.Acylation in benzene, however, gives only II.Reaction of II and III with et

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