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3754-60-7

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3754-60-7 Usage

General Description

1,1'-isopropylidenebis[4-(vinyloxy)benzene] is a chemical compound that is also known as 1,1'-Isopropylidenebis(4-vinyloxybenzene) or Bis(4-(vinyloxy)phenyl)methane. Its molecular formula is C22H22O2 and it has a molecular weight of 318.41 g/mol. 1,1'-isopropylidenebis[4-(vinyloxy)benzene] is used in the production of polymers, resins, and other industrial materials. It is a colorless to pale yellow liquid with a faint, sweet odor. It is considered to be moderately toxic to aquatic organisms and may cause irritation to the skin and eyes upon contact. It is important to handle this chemical with caution and to follow proper safety protocols when working with it.

Check Digit Verification of cas no

The CAS Registry Mumber 3754-60-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,5 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3754-60:
(6*3)+(5*7)+(4*5)+(3*4)+(2*6)+(1*0)=97
97 % 10 = 7
So 3754-60-7 is a valid CAS Registry Number.

3754-60-7SDS

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 1,1'-(2,2-Propanediyl)bis[4-(vinyloxy)benzene]

1.2 Other means of identification

Product number -
Other names Cyclohexanecarbonitrile,1,1'-iminobis

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:3754-60-7 SDS

3754-60-7Downstream Products

3754-60-7Relevant articles and documents

Nucleophilic addition to acetylenes in superbasic catalytic systems: XVIII. Vinylation of phenols and naphthols with acetylene

Trofimov,Oparina,Kolyvanov,Vysotskaya,Gusarova

, p. 188 - 194 (2015/04/14)

Phenols and naphthols react with acetylene in a superbasic system KOH-DMSO forming the corresponding aryl vinyl ethers in up to 80% yields.

Development of a highly efficient catalytic method for synthesis of vinyl ethers

Okimoto, Yoshio,Sakaguchi, Satoshi,Ishii, Yasutaka

, p. 1590 - 1591 (2007/10/03)

A new method for the preparation of alkyl vinyl ethers has been developed. Thus, various types of alkyl vinyl ethers were synthesized by the reaction of alcohols with vinyl acetate under the influence of a catalytic amount of [Ir(cod)Cl]2 combined with Na2CO3 in good to excellent yields. Copyright

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