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13304-56-8

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13304-56-8 Usage

Physical form

white to slightly brown crystalline powder

Molecular weight

328.386 g/mol

Usage

synthesis of organic compounds and pharmaceuticals, building block for dyes, pigments, and specialty chemicals

Therapeutic potential

anti-cancer agent, ability to inhibit cancer cell growth

Fields of application

chemistry, healthcare, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 13304-56-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,0 and 4 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 13304-56:
(7*1)+(6*3)+(5*3)+(4*0)+(3*4)+(2*5)+(1*6)=68
68 % 10 = 8
So 13304-56-8 is a valid CAS Registry Number.

13304-56-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-naphthalen-1-yl-3-phenylinden-1-one

1.2 Other means of identification

Product number -
Other names -

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:13304-56-8 SDS

13304-56-8Downstream Products

13304-56-8Relevant articles and documents

Direct synthesis of indenones from alkenyliron complexes

Butler, Ian R.,Elliott, Joanne E.,Houde, Jean

, p. 1308 - 1311 (2007/10/02)

Alkenyliron complexes have been prepared by the metathesis of dicarbonyl(η5-cyclopentadienyl)iodoiron with arylsubstituted alkenyllithiums.Thermolysis of the product alkenyliron complexes leads to the formation of indenones in good yields.Key w

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