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1364935-79-4

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1364935-79-4 Usage

Physical state at room temperature

White powdery solid

Chemical structure

Cyclopropylmethyl group attached to a phenoxybenzene moiety

Industrial applications

a. Synthesis of pharmaceuticals and organic compounds
b. Production of pesticides, herbicides, and insecticides
c. Manufacturing of specialty chemicals

Potential applications

a. Medicinal chemistry
b. Drug development

Versatility

Diverse industrial and scientific uses

Check Digit Verification of cas no

The CAS Registry Mumber 1364935-79-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,4,9,3 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1364935-79:
(9*1)+(8*3)+(7*6)+(6*4)+(5*9)+(4*3)+(3*5)+(2*7)+(1*9)=194
194 % 10 = 4
So 1364935-79-4 is a valid CAS Registry Number.

1364935-79-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclopropylmethyl-2-phenoxybenzene

1.2 Other means of identification

Product number -
Other names 1-(Cyclopropylmethyl)-2-phenoxybenzene

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:1364935-79-4 SDS

1364935-79-4Downstream Products

1364935-79-4Relevant articles and documents

Suzuki coupling of potassium cyclopropyl- and alkoxymethyltrifluoroborates with benzyl chlorides

Colombel, Virginie,Rombouts, Frederik,Oehlrich, Daniel,Molander, Gary A.

experimental part, p. 2966 - 2970 (2012/06/01)

Efficient Csp3-Csp3 Suzuki couplings have been developed with both potassium cyclopropyl- and alkoxymethyltrifluoroborates. Moderate to good yields have been achieved in the cross-coupling of potassium cyclopropyltrifluoroborate with benzyl chlorides possessing electron-donating or electron-withdrawing substituents. Benzyl chloride was also successfully cross-coupled to potassium alkoxymethyltrifluoroborates derived from primary, secondary, and tertiary alcohols.

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