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4-Pentenoic acid, 3,3-dimethyl-, (3-phenoxyphenyl)methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

60066-51-5

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60066-51-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60066-51-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,0,6 and 6 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 60066-51:
(7*6)+(6*0)+(5*0)+(4*6)+(3*6)+(2*5)+(1*1)=95
95 % 10 = 5
So 60066-51-5 is a valid CAS Registry Number.

60066-51-5SDS

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 (3-phenoxyphenyl)methyl 3,3-dimethylpent-4-enoate

1.2 Other means of identification

Product number -
Other names 3-phenoxybenzyl 3,3-dimethylpent-4-enoate

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:60066-51-5 SDS

60066-51-5Relevant articles and documents

Process for preparing halogenated compounds

-

, (2008/06/13)

A process for preparing halogenated compounds of formula RCY(Z)CH2 CH(X)C(CH3)CH2 COR1 where X, Y and Z are halo, R is alkyl, halo, haloalkyl or aryl, and R1 is hydroxy, halo, alkoxy, alkyl or haloalkyl, or the residue of a pyrethroidal alcohol, in which a compound of formula CH2 =CHC(CH3)2 COR1 is reacted with a sulphonyl halide of formula RCY(Z)SO2 X. The process avoids the use of volatile halocarbons in the production of valuable intermediates for insecticides.

Process for preparing dihalovinylcyclopropanecarboxylates

-

, (2008/06/13)

Novel syntheses of dihalovinylcyclopropanecarboxylates, including potent insecticides, are described. The processes begin with the reaction between an alkenol and an orthoester to produce a γ-unsaturated carboxylate, followed by the catalyzed addition of a carbon tetrahalide to the double bond and dehydrohalogenation to produce a cyclopropane derivative.

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