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4-MYRISTOYLBENZO-15-CROWN-5 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74965-98-3

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74965-98-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74965-98-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,9,6 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 74965-98:
(7*7)+(6*4)+(5*9)+(4*6)+(3*5)+(2*9)+(1*8)=183
183 % 10 = 3
So 74965-98-3 is a valid CAS Registry Number.

74965-98-3SDS

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 4-MYRISTOYLBENZO-15-CROWN-5

1.2 Other means of identification

Product number -
Other names -

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:74965-98-3 SDS

74965-98-3Downstream Products

74965-98-3Relevant academic research and scientific papers

Modified Crown Ether Catalysts. 2. Synthesis of Alkanoyl-, Aroyl-, α-Hydroxyalkyl- and Alkylbenzo and Alkylcyclohexano Crown Ethers

Stott, Paul E.,Bradshaw, Jerald S.,Parish, W. Wesley,Copper, James W.

, p. 4716 - 4720 (2007/10/02)

Improved procedures for the synthesis and purification of alkanoyl- and aroylbenzo crown ethers are reported.Several new alkanoyl- and α-hydroxyalkylbenzo crown ethers were prepared.Alkylbenzo crown ethers were prepared in high yield by the Raney nickel catalyzed hydrogen-transfer reductions of the corresponding acyl- or hydroxyalkylbenzo crown ether compounds.The reduction of the tosylhydrazones of acylbenzo crown ethers with sodium borohydride in acetic acid also yielded the corresponding alkyl derivate.Attempted reduction of the acyl- and α-hydroxyalkylbenzo crown ethers by catalytic hydrogenation over palladium catalysts was unsuccessful apparently due to strong binding of the crown ethers to the catalyst.Alkylcyclohexano crown ethers were prepared by catalytic hydrogenation of the aromatic rings of the corresponding alkylbenzo crown ethers.

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