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100132-04-5

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100132-04-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 100132-04-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,1,3 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 100132-04:
(8*1)+(7*0)+(6*0)+(5*1)+(4*3)+(3*2)+(2*0)+(1*4)=35
35 % 10 = 5
So 100132-04-5 is a valid CAS Registry Number.

100132-04-5SDS

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 2-(2-phenoxyethylamino)ethanol

1.2 Other means of identification

Product number -
Other names 2-(2-Phenoxy-aethylamino)-aethanol

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:100132-04-5 SDS

100132-04-5Relevant articles and documents

NOVEL OXABISPIDINE COMPOUNDS AND THEIR USE IN THE TREATMENT OF CARDIAC ARRHYTHMIAS

-

Page/Page column 68-69, (2008/06/13)

There is provided compounds of formula I, wherein R1, R2, R4, R41 to R46, A, B and G have meanings given in the description, which are useful in the prophylaxis and in the treatment of arrhythmias, in particular atrial and ventricular arrhythmias.

PARTICIPATION OF A NEIGHBORING AMIDE GROUP IN THE HYDROLYTIC C-OAr CLEAVAGE OF N-(ω-PHENOXYALKYL)AMIDES. PART I. N,N-BIS(2-PHENOXYETHYL)PROPIONAMIDE

Dobrzeniecka, Regina

, p. 1135 - 1140 (2007/10/02)

The acid catalyzed hydrolysis of N,N-bis(2-phenoxyethyl)propionamide has been made at 74.8, 84.5 and 94,5 deg C, yielding both bis(2-phenoxyethyl)amine (A) and N,N-(2-phenoxy-2'-hydroxy)diethylamine (B) and phenol.The assistance from the amido group in a displacement of phenol was observed.Kinetic studies have been used to analyze the pathway.The results show that both the amines are formed in two parallel reactions of pseudo-first-order rate constants with kB/kA = 1.20 - 1.77 at 94.5 deg C depending on the concentration of hydrochloric acid.

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