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2476-76-8

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2476-76-8 Usage

Appearance

Yellow crystalline solid

Odor

Distinct aromatic

Usage

a. Synthesis of various organic compounds
b. Building block in pharmaceuticals and agrochemicals production
c. Versatile intermediate in organic chemistry

Unique structure

Useful for creating complex molecules with specific properties

Biological activity

Studied for potential as an anti-cancer agent

Hazardous properties

Can cause skin and eye irritation

Safety precautions

Handle and use with caution

Check Digit Verification of cas no

The CAS Registry Mumber 2476-76-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,7 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2476-76:
(6*2)+(5*4)+(4*7)+(3*6)+(2*7)+(1*6)=98
98 % 10 = 8
So 2476-76-8 is a valid CAS Registry Number.

2476-76-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,6,8-tetramethoxyanthracene-9,10-dione

1.2 Other means of identification

Product number -
Other names 1,3,6,8-tetramethoxyanthra-9,10-quinone

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:2476-76-8 SDS

2476-76-8Relevant articles and documents

Sutherland,Wells

, (1967)

Utilization of Sulfide, Sulfoxide, and Sulfone Groups as Regiochemical Control Elements in the Diels-Alder Reaction of Naphthoquinones

Iwao, Masatomo,Kuraishi, Tsukasa

, p. 4051 - 4060 (2007/10/02)

The Diels-Alder reactions of 2-phenylthio-, 2-phenylsulfinyl-, and 2-phenylsulfonyl-1,4-naphthoquinones, which were unsymmetrically substituted by methoxyl group on the benzenoid ring, with some vinylketene acetals were studied.The regioselectively of the

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