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CAS

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24767-67-7

2-Butanone, 3-chloro-1-phenyl-, also known as chlorophenyl acetone or 1-phenyl-3-chloro-2-butanone, is an organic compound with the chemical formula C10H11ClO. It is a colorless to pale yellow liquid with a molecular weight of 182.65 g/mol. 2-Butanone, 3-chloro-1-phenyl- is characterized by the presence of a chloro substituent at the 3-position and a phenyl group at the 1-position of the butanone backbone. It is used as a synthetic intermediate in the production of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity and potential health hazards, it is important to handle 2-butanone, 3-chloro-1-phenyl- with proper safety measures, including the use of personal protective equipment and proper ventilation.

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  • 24767-67-7 Structure

  • Basic information

    1. Product Name: 2-Butanone, 3-chloro-1-phenyl-
    2. Synonyms:
    3. CAS NO:24767-67-7
    4. Molecular Formula: C10H11ClO
    5. Molecular Weight: 182.65
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 24767-67-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Butanone, 3-chloro-1-phenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Butanone, 3-chloro-1-phenyl-(24767-67-7)
    11. EPA Substance Registry System: 2-Butanone, 3-chloro-1-phenyl-(24767-67-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 24767-67-7(Hazardous Substances Data)

24767-67-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24767-67-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,7,6 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 24767-67:
(7*2)+(6*4)+(5*7)+(4*6)+(3*7)+(2*6)+(1*7)=137
137 % 10 = 7
So 24767-67-7 is a valid CAS Registry Number.

24767-67-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-3-chlorobutan-2-one

1.2 Other means of identification

Product number -
Other names 3-Chlor-1-phenyl-butan-2-on

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:24767-67-7 SDS

24767-67-7Relevant articles and documents

Iridium-catalyzed 1,3-hydrogen shift/chlorination of allylic alcohols

Ahlsten, Nanna,Gomez, Antonio Bermejo,Martin-Matute, Belen

supporting information, p. 6273 - 6276 (2013/07/05)

Tandem: Allylic alcohols react with N-chlorosuccinimide (NCS) in a tandem 1,3-H shift/C-Cl bond formation leading to α-chloroketones and α-chloroaldehydes. The reactions proceed with complete selectivity to give single constitutional isomers of monochlorinated carbonyl compounds. The utility of the transformation is illustrated by the straightforward synthesis of 4,5-disubstituted 2-aminothiazoles from allylic alcohols. Copyright

One-Pot Synthesis of α-Chloro Ketones from Secondary Alcohols Using N,N-Dichloro-p-toluenesulfonamide

Kim, Yong Hae,Lee, In Sang,Lim, Sang Chul

, p. 1125 - 1128 (2007/10/02)

Various alkyl aryl secondary alcohols reacted with N,N-dichloro-p-toluenesulfonamide (N,N-dichloroamine-T) in CH3CN at 35 deg C to give the corresponding α-chloro ketones in excellent yields under mild and neutral conditions.

Metal-Catalyzed Organic Photoreactions. One-Step Synthesis of Chlorinated Ketones from Olefins by Photooxidation in the Presence of Iron(III) Chloride

Kohda, Akira,Ueda, Keiko,,Sato, Tadashi

, p. 509 - 515 (2007/10/02)

Under photooxidation in pyridine in the presence of FeCl3, mono- and disubstituted olefins gave α-chloro ketones, while tri- and tetrasubstituted olefins gave dichloro ketones with a C-C bond cleavage.The reaction was interpreted in terms of an electron-transfer mechanism occurring within the coordination sphere of the iron ion

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