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5-Hexynamide, N-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

155193-71-8

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155193-71-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155193-71-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,1,9 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 155193-71:
(8*1)+(7*5)+(6*5)+(5*1)+(4*9)+(3*3)+(2*7)+(1*1)=138
138 % 10 = 8
So 155193-71-8 is a valid CAS Registry Number.

155193-71-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzylhex-5-ynamide

1.2 Other means of identification

Product number -
Other names 5-Hexynamide,N-(phenylmethyl)

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:155193-71-8 SDS

155193-71-8Relevant academic research and scientific papers

Enzymatic synthesis of N-acylethanolamines: Direct method for the aminolysis of esters

Whitten, Kyle M.,Makriyannis, Alexandros,Vadivel, Subramanian K.

, p. 5753 - 5755 (2012/10/29)

Immobilized Candida antarctica (Novozyme 435) catalyzed synthesis of N-acylethanolamines is described. Treatment of methyl esters with lipase and amines yielded the desired amides within 2-24 h with yields ranging from 41% to 98%.

A photolabile linker for the mild and selective cleavage of enriched biomolecules from solid support

Orth, Ronald,Sieber, Stephan A.

supporting information; experimental part, p. 8476 - 8479 (2010/02/28)

(Chemical Equation Presented) Selective release of enriched biomolecules from solid support is a desirable goal in proteomic and metabolomic studies. Here we demonstrate that photocleavage of a light-sensitive phenacyl ester bond is a suitable alternative

Studies on the Intramolecular Cycloaddition Reaction of Mesoionics Derived from the Rhodium(II)-Catalyzed Cyclization of Diazoimides

Padwa, Albert,Hertzog, Donald L.,Nadler, William R.,Osterhout, Martin H.,Price, Alan T.

, p. 1418 - 1427 (2007/10/02)

A series of alkenyl-substituted imides were prepared by treating the appropriate amide with 2,2,6-trimethyl-4H-1,3-dioxen-4-one in xylene at 140 deg C to give the N-acetoacylated imides.Exposure of these imides to standard diazo transfer conditions gave the desired diazoimides.The carbenoid intermediate derived by treatment of the diazoimide with rhodium(II) acetate undergoes ready cyclization onto the neighboring amide carbonyl oxygen atom to generate an isomuenchnone intermediate.Subsequent 1,3-dipolar cycloaddition across the pendant olefin affords the cycloadduct in high yield.The stereochemical assignment of several of the cycloadducts was deduced by X-ray crystallography.The stereochemical outcome of the reaction is the consequence of an endo cycloaddition of the neighboring ?-bond across the transient isomuenchnone dipole.Molecular mechanics calculations were used to model energy differences between the endo and exo diastereomers.The calculations reveal that the endo diastereomers are significantly (8-12 kcal/mol) lower in energy than the corresponding exo isomers thereby providing a rationale for the preferred endo cycloaddition.Ring opening of the cycloadducts occured readily producing a transient N-acyliminium ion which either lost a proton to give an enamide or was reduced by Et3SiH to afford a bicyclic piperidine ring.

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