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60066-48-0

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60066-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60066-48-0 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, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 60066-48:
(7*6)+(6*0)+(5*0)+(4*6)+(3*6)+(2*4)+(1*8)=100
100 % 10 = 0
So 60066-48-0 is a valid CAS Registry Number.

60066-48-0SDS

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 Benzyl 2-(β,β-dichlorovinyl)-3,3-dimethylcyclopropanecarboxylate

1.2 Other means of identification

Product number -
Other names 2-(β,β-Dichlor-vinyl)-3,3-dimethyl-cyclopropan-carbonsaeure-benzylester

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:60066-48-0 SDS

60066-48-0Downstream Products

60066-48-0Relevant articles and documents

Phase-Transfer Catalyzed Synthesis of Amides and Esters of Carboxylic Acids

Jaszay, Zsuzsa M.,Petnehazy, Imre,Toeke, Laszlo

, p. 745 - 747 (2007/10/02)

A convenient one-pot procedure is reported for the preparation of carboxamides and carboxylic acid esters from carboxylic acids and amines or alcohols, respectively.The carboxylic acids are activated by sulfonyl chlorides under solid-liquid phase-transfer conditions using solid potassium carbonate as base and a lipophilic quaternary ammonium salt as catalyst.

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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