Basic information

Product Name: 2-Cyclopentene-1-carboxylic acid, 4-hydroxy-2-methyl-3-phenyl-, methyl ester
Synonyms:
CAS NO:88579-91-3
Molecular Formula: C14H16O3
Molecular Weight: 232.279
EINECS: N/A
Product Categories: N/A

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: 2-Cyclopentene-1-carboxylic acid, 4-hydroxy-2-methyl-3-phenyl-, methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-Cyclopentene-1-carboxylic acid, 4-hydroxy-2-methyl-3-phenyl-, methyl ester(88579-91-3)
EPA Substance Registry System: 2-Cyclopentene-1-carboxylic acid, 4-hydroxy-2-methyl-3-phenyl-, methyl ester(88579-91-3)

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: 88579-91-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 88579-91-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,5,7 and 9 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 88579-91:
(7*8)+(6*8)+(5*5)+(4*7)+(3*9)+(2*9)+(1*1)=203
203 % 10 = 3
So 88579-91-3 is a valid CAS Registry Number.

88579-91-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name	4-Hydroxy-2-methyl-3-phenyl-cyclopent-2-enecarboxylic acid methyl ester

1.2 Other means of identification

Product number	-
Other names	-

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:88579-91-3 SDS

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88579-91-3Relevant academic research and scientific papers

NEW SYNTHESIS OF CYCLOPENTENOL AND SPIRODECANOL DERIVATIVES VIA INTRAMOLECULAR PHOTO-OXETANE FORMATION

Kim, Tong Hei,Hayase, Yoshio,Isoe, Sachihiko

, p. 1421 - 1424 (2007/10/02)

Cyclopentenol and spirodecanol derivatives accessible to natural products were synthesized in moderate yield by the irradiation of olefinic β-keto esters followed by treatment with sodium hydride.

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