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56298-75-0

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56298-75-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56298-75-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,2,9 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 56298-75:
(7*5)+(6*6)+(5*2)+(4*9)+(3*8)+(2*7)+(1*5)=160
160 % 10 = 0
So 56298-75-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H16/c1-3-12(2)9-8-10-6-4-5-7-11(10)12/h4-7H,3,8-9H2,1-2H3

56298-75-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethyl-3-methyl-1,2-dihydroindene

1.2 Other means of identification

Product number -
Other names 1-Aethyl-1-methyl-indan

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:56298-75-0 SDS

56298-75-0Downstream Products

56298-75-0Relevant articles and documents

Ru(III)-Catalyzed Cyclization of Arene-Alkene Substrates via Intramolecular Electrophilic Hydroarylation

Youn, So Won,Pastine, Stefan J.,Sames, Dalibor

, p. 581 - 584 (2007/10/03)

(Matrix presented) We herein report that RuCl3/AgOTf has proven to be a hydroarylation catalyst with an efficiency and scope superior to previously known methods. This catalyst demonstrated consistent performance with arene-ene substrates of diverse structural features, providing good to excellent yields of cyclization products (chromanes, tetralins, terpenoids, dihydrocoumarins).

INTRAMOLECULAR CYCLOALKYLATION OF PHENYLALKANOLS IN THE PRESENCE OF SULFURIC ACID

Sakhabutdinov, A.G.,Usmanova, A.G.,Proidakov, A.G.,Bazhenov, B.A.,Schmidt, F.K.

, p. 1525 - 1529 (2007/10/02)

Te distribution of the deuterium in the benzocyclenes formed during the intermolecular cycloalkylation of 2-R-4-phenyl-2-butanol (R=CD3, CD2CH3, CH2CD3) in the presence of 85percent sulfuric acid was investigated by NMR spectroscopy and mass spectrometry.Hydrogen exchange takes place at the stage of formation of the γ-phenylalkyl cation, the average lifetime of which is sufficient for the establishment of an isotopic equilibrium by successive elimination addition of an deuteron.

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