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Benzene, 1,1'-(1-ethoxyethylidene)bis- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35036-32-9

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35036-32-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35036-32-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,0,3 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 35036-32:
(7*3)+(6*5)+(5*0)+(4*3)+(3*6)+(2*3)+(1*2)=89
89 % 10 = 9
So 35036-32-9 is a valid CAS Registry Number.

35036-32-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (1-ethoxy-1-phenylethyl)benzene

1.2 Other means of identification

Product number -
Other names 1-Ethoxy-1,1-diphenylethan

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:35036-32-9 SDS

35036-32-9Downstream Products

35036-32-9Relevant academic research and scientific papers

Cerium(IV), as a selective and efficient catalyst for alcoholyses of allylic and tertiary benzylic alcohols

Iranpoor, Nasser,Mothaghineghad, Enayatholah

, p. 1859 - 1870 (2007/10/02)

An efficient and selective method is described for the catalytic conversion of allylic, and tertiary benzylic alcohols into their corresponding ethers in the presence of Ce(IV) under solvolytic and non- solvolytic conditions.

ARYL REARRANGEMENT ON THE PHOTOLYSIS OF 2-ARYL-2-ETHOXY-2-PHENYLETHYL CABALOXIME.

Tada,Inoue,Okabe

, p. 1420 - 1423 (2007/10/02)

The photolysis of 2-aryl-2-ethoxy-2-phenylethyl cobaloxime followed by hydrolysis gave two kinds of substituted 1,2-diphenylethanones arising via phenyl or substituted-phenyl migration. The substituent effect on the aryl rearrangement is similar to that on the reported neophyl rearrangement, and the rearrangement takes place by a radical mechanism without the deep involvement of cobaloxine(II).

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