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38731-83-8

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38731-83-8 Usage

Chemical structure

Xanthene core with two methyl groups at the 1 and 3 positions

Usage

Building block in the synthesis of fluorescent dyes and pigments

Investigation

Potential use in photodynamic therapy for cancer treatment

Research focus

Photochemical and photophysical properties

Field of interest

Photochemistry and materials science

Industry relevance

Valuable compound in the chemical industry

Scientific research

Important for research in photochemistry and materials science

Aromatic structure

Contributes to its stability and potential applications

Derivatives

Xanthenone derivatives are being studied for various applications

Check Digit Verification of cas no

The CAS Registry Mumber 38731-83-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,7,3 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38731-83:
(7*3)+(6*8)+(5*7)+(4*3)+(3*1)+(2*8)+(1*3)=138
138 % 10 = 8
So 38731-83-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H14O/c1-10-7-11(2)13-9-12-5-3-4-6-14(12)16-15(13)8-10/h3-8H,9H2,1-2H3

38731-83-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dimethyl-9H-xanthene

1.2 Other means of identification

Product number -
Other names 1,3-Dimethyl-xanthin

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:38731-83-8 SDS

38731-83-8Downstream Products

38731-83-8Relevant articles and documents

Lewis acid-catalysed one pot synthesis of substituted xanthenes

Boe, Esther,Hillringhaus, Tim,Nitsch, Jacqueline,Klussmann, Martin

, p. 1744 - 1748 (2011)

A direct synthesis of substituted xanthenes from salicylaldehydes and cyclohexenones or tetralones has been developed. The reaction is catalysed by Lewis acids like scandium triflate and furnishes substituted xanthenes in good to excellent yields using either microwave or thermal heating. Microwave heating results in significantly shortened reaction times of 30 min and generally higher yields.

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