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35135-43-4

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35135-43-4 Usage

Molecular Weight

310.43 g/mol

Structure

A benzene ring with a methoxy group at the first position, and a 2-(E)-2-[4-(pentyloxy)phenyl]ethenyl substituent at the second position.

Substituent

A pentyloxy group attached to a phenyl ring, which is further connected to an ethenyl group.

Class

Benzene derivatives

Usage

Commonly used in organic synthesis and pharmaceutical research due to its unique structure and potential biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 35135-43-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,3 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 35135-43:
(7*3)+(6*5)+(5*1)+(4*3)+(3*5)+(2*4)+(1*3)=94
94 % 10 = 4
So 35135-43-4 is a valid CAS Registry Number.

35135-43-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methoxy-2-[2-(4-pentoxyphenyl)ethenyl]benzene

1.2 Other means of identification

Product number -
Other names 4-Methoxy-4'-pentoxy-trans-stilben

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:35135-43-4 SDS

35135-43-4Downstream Products

35135-43-4Relevant articles and documents

Synthesis of alkyloxy stilbenes by one-pot O-alkylation-Wittig and O-alkylation-Wittig-Heck reaction sequence

Patel, Krupa N.,Kamath, Bola V.,Bedekar, Ashutosh V.

, p. 80 - 84 (2013/02/21)

A new route for the synthesis of alkyloxy stilbenes from hydroxy benzaldehydes is developed by a combination of one-pot reactions. Tandem one-pot O-alkylation-Wittig and O-alkylation-Wittig-Heck reactions offer a simple access to conjugated alkyloxy stilbenes. A highly conjugated tetra(p-alkyloxystyryl)benzene was synthesized from 1,2,4,5-tetrabromobenzene involving a series of one-pot operations following the O-alkylation-Wittig-Heck scheme.

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