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66064-61-7

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66064-61-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66064-61-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,0,6 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 66064-61:
(7*6)+(6*6)+(5*0)+(4*6)+(3*4)+(2*6)+(1*1)=127
127 % 10 = 7
So 66064-61-7 is a valid CAS Registry Number.

66064-61-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-bis(4-methoxyphenyl)indene-1,3-dione

1.2 Other means of identification

Product number -
Other names 2,2-di-para-methoxyphenyl-1,3-indanedione

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:66064-61-7 SDS

66064-61-7Relevant articles and documents

A study on the friedel-crafts type reaction of ninhydrin with arenes

Song, Hyun Nam,Seong, Mi Ra,Son, Ji Suk,Kim, Jae Nyoung

, p. 1865 - 1870 (1998)

The reactions of ninhydrin (1, 1,2,3-indantrione) with arenes in the presence of concentrated sulfuric acid afforded mono- or di-substituted ninhydrin derivatives at the 2-position in reasonable yields.

Facile acid-catalyzed condensation of ninhydrin with enols and aromatic compounds and microwave enhanced condensation of ninhydrin with hydroxy aromatic systems in solid state

Kundu, Sandip Kumar,Patra, Amarendra,Pramanik, Animesh

, p. 604 - 611 (2007/10/03)

Di- and trihydroxybenzenes, 2,6-dihydroxyacetophenone, α- and β-naphthols and also 3- and 4-hydroxycoumarins and various enols smoothly condense with ninhydrin in HOAc medium giving 2-substituted 1,3-dioxoindanes. Monoarylated products were also obtained

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