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132560-67-9

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132560-67-9 Usage

Synonym

4'-propylacetophenone

+ Physical state

Liquid

+ Appearance

Colorless to pale yellow liquid

+ Molecular weight

212.7 g/mol

+ Boiling point

299-301°C (574-578°F)

+ Melting point

Not applicable (decomposes)

+ Solubility

Slightly soluble in water, miscible with organic solvents

+ Functional groups

Ketone, chloro, alkyl

+ Aromatic ring

Phenyl group with a propyl group attached at the 4-position

Uses

+ Intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds
+ Flavoring agent and fragrance in the food and cosmetic industries

Hazards

+ Classified as a hazardous substance
+ Potential harmful effects on human health and the environment
+ Handling precautions are necessary

Check Digit Verification of cas no

The CAS Registry Mumber 132560-67-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,5,6 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 132560-67:
(8*1)+(7*3)+(6*2)+(5*5)+(4*6)+(3*0)+(2*6)+(1*7)=109
109 % 10 = 9
So 132560-67-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H15ClO/c1-3-4-10-5-7-11(8-6-10)12(14)9(2)13/h5-9H,3-4H2,1-2H3

132560-67-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-chloro-1-(4-propylphenyl)propan-1-one

1.2 Other means of identification

Product number -
Other names 1-Propanone,2-chloro-1-(4-propylphenyl)

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:132560-67-9 SDS

132560-67-9Relevant articles and documents

Photochemical Rearrangement of α-Chloro-Propiophenones to α-Arylpropanoic Acids: Studies on Chirality Transfer and Synthesis of (S)-(+)-Ibuprofen and (S)-(+)-Ketoprofen

Sonawane, Harikisan,Bellur, Nanjundiah S.,Kulkarni, Dilip G.,Ayyangar, Nagaraj R.

, p. 1243 - 1260 (2007/10/02)

A new single-step efficient photochemical approach for α-arylpropanoic acids (4) from α-chloro-propiophenones (5) is described.It involves carbonyl triplet excited state directed 1,2-aryl migration of the aryl group which has been found to be highly dependent upon the nature of the aryl substituent.The mode of the rearrangement is probed by the study of the photobehaviour of a set of optically active α-chloro-propiophenones.The results suggest that the nature of the carbonyl triplets (n, ?*/ ?, ?*) plays an important role in the chirality transfer.This method finds application in the synthesis of optically active ibuprofen (4e) and ketoprofen (26), though in moderate optical yields.

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