Basic information

Product Name: 2-Cyclopenten-1-one, 4-hexyl-2-phenyl-
Synonyms:
CAS NO:62156-60-9
Molecular Formula: C17H22O
Molecular Weight: 242.361
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-Cyclopenten-1-one, 4-hexyl-2-phenyl-(CAS DataBase Reference)
NIST Chemistry Reference: 2-Cyclopenten-1-one, 4-hexyl-2-phenyl-(62156-60-9)
EPA Substance Registry System: 2-Cyclopenten-1-one, 4-hexyl-2-phenyl-(62156-60-9)

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: 62156-60-9(Hazardous Substances Data)

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62156-60-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62156-60-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,1,5 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 62156-60:
(7*6)+(6*2)+(5*1)+(4*5)+(3*6)+(2*6)+(1*0)=109
109 % 10 = 9
So 62156-60-9 is a valid CAS Registry Number.

62156-60-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name	4-hexyl-2-phenylcyclopent-2-en-1-one

1.2 Other means of identification

Product number	-
Other names	2-Cyclopenten-1-one,4-hexyl-2-phenyl

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:62156-60-9 SDS

62156-60-9Upstream product

111-66-0 oct-1-ene

62156-60-9Downstream Products

62156-60-9Relevant academic research and scientific papers

STERIC CONTROL IN THE PAUSON CYCLOADDITION: FURTHER SUPPORT FOR THE PROPOSED MECHANISM

Krafft, Marie E.

, p. 999 - 1002 (1988)

Dicobalthexacarbonyl complexes of internal alkynes react with olefins to give cyclopentenones with a high degree of regiocontrol.Analogous reactions of terminal alkynes give rise to regioisomeric mixtures of cyclopentenones.

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