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100618-31-3

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100618-31-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100618-31-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,6,1 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 100618-31:
(8*1)+(7*0)+(6*0)+(5*6)+(4*1)+(3*8)+(2*3)+(1*1)=73
73 % 10 = 3
So 100618-31-3 is a valid CAS Registry Number.

100618-31-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl N-(4-phenylbutyl)carbamate

1.2 Other means of identification

Product number -
Other names (4-Phenyl-butyl)-carbamidsaeure-aethylester

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:100618-31-3 SDS

100618-31-3Downstream Products

100618-31-3Relevant articles and documents

Evaluation of ethyl: N -(2-phenethyl) carbamate analogues as biofilm inhibitors of methicillin resistant Staphylococcus aureus

Stephens, Matthew D.,Yodsanit, Nisakorn,Melander, Christian

, p. 6853 - 6856 (2016/07/21)

A small molecule library consisting of 45 compounds was synthesized based on the bacterial metabolite ethyl N-(2-phenethyl) carbamate. Screening of the compounds revealed a potent analogue capabale of inhibiting several strains of Methicillin Resistant S. aureus biofilms with low to moderate micromolar IC50 values.

Process for the preparation of N,o-substituted mono-and/or polyurethanes

-

, (2008/06/13)

The invention describes a process for the preparation of N,o-substituted mono- and/or polyurethanes of formula in which R1 is an aliphatic, cycloaliphatic, aromatic, araliphatic, or heterocyclic radical, which may be substituted, R2 is an aliphatic, cycloaliphatic, or araliphatic radical which may be substituted with alkoxy or polyoxyalkylene groups, and is a whole number from 1 to 5, through the reaction of N-substituted allophanates and/or polyallophanates with alcohols R2 OH in the presence or absence of catalysts at temperatures of at least 160° C., preferably from 165° to 250° C.

Process for the preparation of an aryl mono-, di-, and/or polyurethane

-

, (2008/06/13)

A process for the preparation of an aryl-mono and/or polyurethane comprising the steps of A. reacting a primary aromatic mono, di-, and/or polyamine with an O-alkyl carbamate in the presence of alcohol and catalysts, and B. separating the ammonia and other by-products from the aliphatic and/or cycloaliphatic di- and/or polyurethane. The reaction is preferably carried out in the presence of urea. The aryl mono-, di-, and/or polyurethanes produced are valuable end and intermediate products. They can be transferred into the corresponding isocyanates which can then be used for the preparation of polyurethanes.

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