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24301-50-6

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24301-50-6 Usage

Derivative of

Anthracene

Functional groups

Two acetoxy groups attached at the 1 and 4 positions

Applications

a. Production of dyes, pigments, and fluorescent materials
b. Organic synthesis
c. Research as a reagent for various chemical reactions

Physical state

Solid

Solubility

a. Insoluble in water
b. Soluble in organic solvents

Toxicity

Moderately toxic

Hazards

Skin and eye irritant

Importance

Significant compound in organic chemistry and materials science

Check Digit Verification of cas no

The CAS Registry Mumber 24301-50-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,0 and 1 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 24301-50:
(7*2)+(6*4)+(5*3)+(4*0)+(3*1)+(2*5)+(1*0)=66
66 % 10 = 6
So 24301-50-6 is a valid CAS Registry Number.
InChI:InChI=1/C18H14O4/c1-11(19)21-17-7-8-18(22-12(2)20)16-10-14-6-4-3-5-13(14)9-15(16)17/h3-10H,1-2H3

24301-50-6SDS

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 (4-acetyloxyanthracen-1-yl) acetate

1.2 Other means of identification

Product number -
Other names anthracene-1,4-diyl diacetate

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:24301-50-6 SDS

24301-50-6Relevant articles and documents

Neopentylation of Phenols and Hydroquinones

Quast, Helmut,Schulze, Johannes

, p. 509 - 512 (2007/10/02)

Neopentylation of phenol, the hydroquinones 6 as well as the hydroquinone diacetates 8 by means of neopentyl iodide in diethylene glycol dimethyl ether in the presence of cesium carbonate affords high yields of the neopentyl ethers 2a and 7, respectively.

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