Basic information

Product Name: 1-Cyclohexene-1-carboxylic acid, 4-hydroxy-2-methyl-, ethyl ester
Synonyms:
CAS NO:62327-18-8
Molecular Formula: C10H16O3
Molecular Weight: 184.235
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: 1-Cyclohexene-1-carboxylic acid, 4-hydroxy-2-methyl-, ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1-Cyclohexene-1-carboxylic acid, 4-hydroxy-2-methyl-, ethyl ester(62327-18-8)
EPA Substance Registry System: 1-Cyclohexene-1-carboxylic acid, 4-hydroxy-2-methyl-, ethyl ester(62327-18-8)

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: 62327-18-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 62327-18-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,3,2 and 7 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 62327-18:
(7*6)+(6*2)+(5*3)+(4*2)+(3*7)+(2*1)+(1*8)=108
108 % 10 = 8
So 62327-18-8 is a valid CAS Registry Number.

62327-18-8SDS

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	ethyl 4-hydroxy-2-methylcyclohexene-1-carboxylate

1.2 Other means of identification

Product number	-
Other names	1-Cyclohexene-1-carboxylic acid,4-hydroxy-2-methyl-,ethyl ester

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:62327-18-8 SDS

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62327-18-8Relevant academic research and scientific papers

The reaction of ketone enolates with a δ-oxo phosphonate: A carbanion-based [4+2] annulation

Kraus,Jones

, p. 793 - 794 (2001)

The reaction of ketone enolates with phosphonate aldehyde 3 followed by acetylation and cyclization represents a useful carbanion-based strategy for the appendage of a functionalized six-membered ring.

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