Basic information

Product Name: 2-Pentanone, 5-(2-hydroxy-4,6-dimethylphenyl)-
Synonyms:
CAS NO:96358-77-9
Molecular Formula: C13H18O2
Molecular Weight: 206.285
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-Pentanone, 5-(2-hydroxy-4,6-dimethylphenyl)-(CAS DataBase Reference)
NIST Chemistry Reference: 2-Pentanone, 5-(2-hydroxy-4,6-dimethylphenyl)-(96358-77-9)
EPA Substance Registry System: 2-Pentanone, 5-(2-hydroxy-4,6-dimethylphenyl)-(96358-77-9)

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: 96358-77-9(Hazardous Substances Data)

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96358-77-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96358-77-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,3,5 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 96358-77:
(7*9)+(6*6)+(5*3)+(4*5)+(3*8)+(2*7)+(1*7)=179
179 % 10 = 9
So 96358-77-9 is a valid CAS Registry Number.

96358-77-9SDS

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	5-(2-hydroxy-4,6-dimethylphenyl)pentan-2-one

1.2 Other means of identification

Product number	-
Other names	2-Pentanone,5-(2-hydroxy-4,6-dimethylphenyl)

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:96358-77-9 SDS

96358-77-9Upstream product

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96358-77-9Relevant academic research and scientific papers

Synthesis of rac-Cinera-5,7,11-trien-9-one

Bohlmann, Ferdinand,Krueger, Martin

, p. 560 - 565 (2007/10/02)

The spiro trienone 22 isolated from a Cineraria species has been synthesized as racemate by intramolecular alkylation starting with 5-isopropyl-3-methylphenol via a suitable phenol substituted in position 2.This compound gave no Diels-Alder reaction with

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