Basic information

Product Name: Benzeneacetic acid, a-hydroxy-a-methyl-4-phenoxy-
Synonyms: 2-Hydroxy-2-(4-phenoxyphenyl)propanoicacid
CAS NO:157874-97-0
Molecular Formula: C15H14 O4
Molecular Weight: 258.274
EINECS: N/A
Product Categories: N/A
Mol File: 157874-97-0.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Benzeneacetic acid, a-hydroxy-a-methyl-4-phenoxy-(CAS DataBase Reference)
NIST Chemistry Reference: Benzeneacetic acid, a-hydroxy-a-methyl-4-phenoxy-(157874-97-0)
EPA Substance Registry System: Benzeneacetic acid, a-hydroxy-a-methyl-4-phenoxy-(157874-97-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 157874-97-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 157874-97-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,7,8,7 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 157874-97:
(8*1)+(7*5)+(6*7)+(5*8)+(4*7)+(3*4)+(2*9)+(1*7)=190
190 % 10 = 0
So 157874-97-0 is a valid CAS Registry Number.

157874-97-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name	2-hydroxy-2-(4-phenoxyphenyl)propanoic acid

1.2 Other means of identification

Product number	-
Other names	2-Hydroxy-2-(4-phenoxyphenyl)propansaeure

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).

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157874-97-0Relevant academic research and scientific papers

Synthesis and properties of 3-alkylsubstituted 1-alkoxy(hydroxy)indolin-2-ones

Geffken,Frobose

, p. 889 - 893 (2007/10/02)

N-alkoxy-2-aryl-2-hydroxycarboxamides 3 are smoothly converted into 3-alkylsubstituted 1-alkoxyindolin-2-ones (2A) by dicyclohexylcarbodiimide in boiling trichloroethene. The acidolysis of the 1-tert-butoxyindolin-2-ones 2Ab, g, i, k as well as the 1-alko

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