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79034-12-1

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79034-12-1 Usage

Classification

Substituted indane derivative, Aromatic hydrocarbons

Physical appearance

Colorless to pale yellow liquid

Odor

Sweet, floral

Primary use

Fragrance ingredient in perfumes, soaps, and personal care products

Potential applications

Pharmaceuticals, Agrochemicals

Safety precautions

Potential hazards, proper safety measures required when handling and using

Check Digit Verification of cas no

The CAS Registry Mumber 79034-12-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,0,3 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79034-12:
(7*7)+(6*9)+(5*0)+(4*3)+(3*4)+(2*1)+(1*2)=131
131 % 10 = 1
So 79034-12-1 is a valid CAS Registry Number.
InChI:InChI=1/C16H16/c1-16(14-8-3-2-4-9-14)12-11-13-7-5-6-10-15(13)16/h2-10H,11-12H2,1H3

79034-12-1SDS

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 3-methyl-3-phenyl-1,2-dihydroindene

1.2 Other means of identification

Product number -
Other names 1-methyl-1-phenyl-2,3-dihydro-1h-indene

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:79034-12-1 SDS

79034-12-1Relevant articles and documents

Metal-Free Domino One-Pot Decarboxylative Cyclization of Cinnamic Acid Esters: Synthesis of Functionalized Indanes

Gopi Krishna Reddy, Alavala,Satyanarayana, Gedu

, p. 12212 - 12222 (2016/12/23)

Trifluoroacetic acid promoted unprecedented domino reaction for the synthesis of diverse indanes starting from simple cinnamic acid esters is described. Their formation can be explained via acid triggered decarboxylation of cinnamic acid esters and subsequent inter/intramolecular cyclization. Overall process involves in the intramolecular cleavage of two σ-bonds (C-O and C-C) and inter/intramolecular construction of two/one C-C σ-bond(s). Significantly, this protocol was successful without the aid of any metal salts.

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