Welcome to LookChem.com Sign In|Join Free
  • or
1,1,2-trimethyl-3-phenyl-2,3-dihydro-1H-indene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33508-02-0

Post Buying Request

33508-02-0 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

33508-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33508-02-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,5,0 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 33508-02:
(7*3)+(6*3)+(5*5)+(4*0)+(3*8)+(2*0)+(1*2)=90
90 % 10 = 0
So 33508-02-0 is a valid CAS Registry Number.

33508-02-0SDS

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 2,3,3-trimethyl-1-phenyl-1,2-dihydroindene

1.2 Other means of identification

Product number -
Other names 1,1,2-TRIMETHYL-3-PHENYLINDAN

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:33508-02-0 SDS

33508-02-0Downstream Products

33508-02-0Relevant academic research and scientific papers

A novel efficient method for the synthesis of substituted olefins; Cross coupling of two different alcohols using NaHSO4/SiO2

Aoyama, Tadashi,Koda, Shuichi,Takeyoshi, Yuka,Ito, Tetsuhiro,Takido, Toshio,Kodomari, Mitsuo

, p. 6605 - 6607 (2013/07/26)

Simple and efficient cross coupling of alcohols was developed in the presence of NaHSO4/SiO2 to give the corresponding substituted olefins. Direct coupling of alcohols and alkenes was also achieved to give substituted olefins. NaHSO4/SiO2 could be recycled 7 times without loss of catalytic activity.

Relative Reactivities of Alkyl-Substituted Alkenes and Cycloalkenes towards Diarylcarbenium Ions

Mayr, Herbert,Pock, Rudolf

, p. 2473 - 2496 (2007/10/02)

The relative reactivities of alkyl-substituted alkenes 4 towards diarylmethyl cations 2 generated in situ from diarylmethyl chlorides 1 and Lewis acids were determined by competition experiments.The relative reactivities were almost independent of the nature of the Lewis acid. Eventual differences of the solvation free enthalpies of various activated complexes are, therefore, independent of the nature of the gegen ions.The rate acceleration by methyl groups - 6-50 by CH3 at the attacked vinylic position and approximately 104 at the developing carbenium centre - indicates a scarcely bridged transition state.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 33508-02-0