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106116-41-0

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106116-41-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 106116-41-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,1,1 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 106116-41:
(8*1)+(7*0)+(6*6)+(5*1)+(4*1)+(3*6)+(2*4)+(1*1)=80
80 % 10 = 0
So 106116-41-0 is a valid CAS Registry Number.

106116-41-0SDS

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 2-(3,5-Dimethylbenzyliden)-2,3-dihydro-5,7-dimethyl-1H-inden-1-on

1.2 Other means of identification

Product number -
Other names 2-[1-(3,5-Dimethyl-phenyl)-meth-(E)-ylidene]-5,7-dimethyl-indan-1-one

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:106116-41-0 SDS

106116-41-0Relevant articles and documents

Benzoannelated Centropolyquinanes, 3. - Synthesis of Multiply Substituted Triptindans (9H,10H-4b,9a-(Benzenomethano)indenoindenes) with Substituents in their Molecular Cavity

Kuck, Dietmar,Paisdor, Bernd,Gruetzmacher, Hans-Friedrich

, p. 589 - 596 (2007/10/02)

The synthesis of triptindans 13a-e substituted by methoxy and/or methyl groups in positions 2,4,5,7,13, and 15 has been achieved by acid-catalysed cyclodehydration of the corresponding 2,2-dibenzyl-1-indanones 12a-e using Amberlyst 15 and polyphosphoric acid, respectively.Total demethylation of 13a followed by selective deoxygenation of the resulting hexahydroxy compound 14 affords the 4,5,15-trihydroxytriptindan (17) (4, R = OH) bearing the three substituents in its molecular cavity.

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