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N,N-bis(2-hydroxyethyl)-2-phenylacetamide, also known as Phenol Red, is an organic compound with the chemical formula C19H20N2O4. It is a colorless, crystalline solid that is soluble in water, alcohol, and ether. Phenol Red is widely used as a pH indicator in acid-base titrations, with a color change range from yellow (pH 6.8) to red (pH 8.4). It is also employed as a biological stain, a dye in the pharmaceutical industry, and a reagent in various chemical analyses. The compound is synthesized by reacting 2-phenylacetic acid with ethylene oxide, followed by the addition of ammonia. Due to its potential health risks, including irritation and sensitization, Phenol Red is classified as a hazardous substance and requires proper handling and disposal.

7147-91-3

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7147-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7147-91-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7147-91:
(6*7)+(5*1)+(4*4)+(3*7)+(2*9)+(1*1)=103
103 % 10 = 3
So 7147-91-3 is a valid CAS Registry Number.

7147-91-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-bis(2-hydroxyethyl)-2-phenylacetamide

1.2 Other means of identification

Product number -
Other names Phenyl-essigsaeure-[bis-(2-hydroxy-aethyl)-amid]

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:7147-91-3 SDS

7147-91-3Downstream Products

7147-91-3Relevant academic research and scientific papers

Ammonium nitrate: A biodegradable and efficient catalyst for the direct amidation of esters under solvent-free conditions

Ramesh, Perla,Fadnavis, Nitin W.

supporting information, p. 138 - 140 (2015/02/19)

A simple, metal-free, and environment-friendly procedure is developed for the direct conversion of esters to amides using ammonium nitrate as a catalyst under solvent-free conditions. Aryls, heteroaryls, and aliphatic esters are easily converted to the corresponding amides in excellent isolated yields (85-99%). An enantiopure ester and amine were both shown to react without racemization. The methodology has been successfully applied to preparation of procainamide.

Carboxyl activation of 2-mercapto-4,6-dimethylpyrimidine through n-acyl-4,6-dimethylpyrimidine-2-thione: A chemical and spectrophotometric investigation

Rajan

, p. 287 - 291 (2015/01/30)

2-Mercapto-4,6-dimethylpyrimidine, as effective carboxyl activating group, has been successfully proved by converting it into respective acyl derivatives and the subsequent conversion to the amides and esters respectively using amines, amino alcohols and alcohols. The aminolysis and esterification were monitored chemically and spectrophotometrically. This paved way to establish that the above mercaptopyrimidine derivative is an efficient carboxyl activating group applicable in solid phase peptide synthesis.

Carboxyl activation of 3-mercapto-5,6-diphenyl-1,2,4-triazine through N-phenylacetyl-5,6-diphenyl-1,2,4-triazine-3-thione

Rajan

, p. 119 - 126 (2019/01/21)

The carboxyl activation ability of 3-mercapto-5,6-diphenyl-1,2,4-triazine has been established by coverting it into N-phenylacetyl-5,6-diphenyl-1,2,4-triazine-3-thione and this was then subjected to aminolysis and esterification with amines and alcohols respectively and selective aminolysis with aminoalcohols-monitoring chemically and confirmed spectrophotometrically by UV-Visible scannings. It could be proved that 3- mercapto-5,6-diphenyl-1,2,4-triazine is an efficient carboxyl activating group which can be successfully applied in solid phase peptide synthesis.

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