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1-benzyl-4-propylbenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62155-41-3

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62155-41-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62155-41-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,5 and 5 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62155-41:
(7*6)+(6*2)+(5*1)+(4*5)+(3*5)+(2*4)+(1*1)=103
103 % 10 = 3
So 62155-41-3 is a valid CAS Registry Number.

62155-41-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Propyldiphenylmethane

1.2 Other means of identification

Product number -
Other names Benzene, 1-(phenylmethyl)-4-propyl-

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:62155-41-3 SDS

62155-41-3Downstream Products

62155-41-3Relevant academic research and scientific papers

Friedel-Crafts benzylation of arenes using FeCI3 impregnated montmorillonite K10

Pai,Bajpai,Deshpande,Samant

, p. 2267 - 2273 (2007/10/03)

FeCI3 impregnated Montmorillonite K10 was found to catalyze the Friedel-Crafts benzylation of arenes. Monobenzylation, with the para isomer predominating, was achieved with trace amounts of dibenzylated product.

Environmentally Friendly Chemistry using Supported Reagent Catalysts: Structure-Property Relationships for Clayzic

Clark, James H.,Cullen, Stephen R.,Barlow, Simon J.,Bastock, Tony W.

, p. 1117 - 1130 (2007/10/02)

Supported reagents have been widely used in organic synthesis for some 25 years and their importance is likely to increase as a result of new environmental legislation and the drive towards clean technology.While many supported reagents are stoichiometric in reactions the successful development of genuinely catalytic materials greatly enhances their value especially in liquid phase, typically fine chemical syntheses.Achieving an understanding of the nature of these fascinating materials is also an important aspect of their development and is essential if their true potential is to be realised.Solid acids are the most widely studied of supported reagents and their use as more environmentally acceptable replacements for conventional Broensted and Lewis acids is likely to become increasingly important.Clayzic is a good example of an evironmentally friendly catalyst with particular value as an alternative to the hazardous reagent aluminium chloride in Friedel-Crafts reactions.The structure and properties of this catalyst are, however, poorly understood.X-Ray diffraction studies show that thermal treatment of either clayzic or its base material K10 results in the loss of any montmorillonite crystallinity that remained after the acid treatment of tonsil 13 used to form K10.Thermal treatment of clayzic also results in a steady increase in the surface area of the material.While this is also consistent with structural changes the increase is also likely to be partly due to the dehydration allowing the non-polar adsorbate to enter more of the polar regions of the material.These polar regions can be identified as mesopores created by the acid treatment of the clay and in which the zinc ions largely reside.Spectroscopic titration of the acid sites in clayzic show these to be largely Lewis acid in character.Thus clayzic owes its remarkable Friedel-Crafts activity to the presence of high local concentrations of zinc ions in structural mesopores.Relative reaction rates for the clayzic catalysed benzylation of alkylbenzenes also reveal the importance of these highly polar mesopores.Considerable rate enhancements can be achieved by thermally activating the catalyst and this can be largely attributed to the dehydration of the catalyst enabling better partitioning of the alkylbenzenes into the mesopores.Clayzic can be considered as being a large pore molecular sieve but where the sieving of molecules is controlled more by molecular polarities/polarisibilities than by molecular shape.

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