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6-methyl-1-(propan-2-yl)-2,3-dihydro-1H-indene is an organic compound with the molecular formula C13H18. It is a derivative of the indene family, characterized by a fused benzene and cyclopentane ring system. The compound features a methyl group at the 6th position, a propyl group attached to the 1st position, and a hydrogen atom at the 2nd position. The structure is further stabilized by the presence of a double bond between the 2nd and 3rd carbon atoms, which is part of the dihydro-indene framework. This chemical is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, owing to its unique structure and reactivity.

828-97-7

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828-97-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 828-97-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 828-97:
(5*8)+(4*2)+(3*8)+(2*9)+(1*7)=97
97 % 10 = 7
So 828-97-7 is a valid CAS Registry Number.

828-97-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-methyl-1-propan-2-yl-2,3-dihydro-1H-indene

1.2 Other means of identification

Product number -
Other names 1H-Indene,2,3-dihydro-6-methyl-1-propan-2-yl

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:828-97-7 SDS

828-97-7Downstream Products

828-97-7Relevant academic research and scientific papers

Steric Effects in the Synthesis of 1,7-Dialkylindans

Budhram, Ronald S.,Palaniswamy, Ventakapuran A.,Eisenbraun, Edmund J.

, p. 1402 - 1406 (2007/10/02)

Synthesis routes to 1-alkyl(CH3,C2H5,i-C3H7)-6-methylindans and 1-alkyl(CH3,C2H5,i-C3H7)-7-methylindans are described.Members of the latter series, especially 1-isopropyl-7-methylindan, are sterically hindered through a peri interaction.This effect manifests itself throughout the study and necessitated use of alternative synthesis routes.Yields in the Grignard, Peterson olefination, Reformatsky, and Wittig reactions as well as catalytic hydrogenation and Li/NH3 reduction of α,β-unsaturated acids were compared.

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