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3-chloro-1-(3,4-dimethylphenyl)propan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 22422-23-7 Structure
  • Basic information

    1. Product Name: 3-chloro-1-(3,4-dimethylphenyl)propan-1-one
    2. Synonyms: 3-chloro-1-(3,4-dimethylphenyl)propan-1-one
    3. CAS NO:22422-23-7
    4. Molecular Formula: C11H13ClO
    5. Molecular Weight: 196.67
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 22422-23-7.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 315.8°Cat760mmHg
    3. Flash Point: 166.6°C
    4. Appearance: /
    5. Density: 1.084g/cm3
    6. Vapor Pressure: 0.000428mmHg at 25°C
    7. Refractive Index: 1.522
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-chloro-1-(3,4-dimethylphenyl)propan-1-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-chloro-1-(3,4-dimethylphenyl)propan-1-one(22422-23-7)
    12. EPA Substance Registry System: 3-chloro-1-(3,4-dimethylphenyl)propan-1-one(22422-23-7)
  • 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: 22422-23-7(Hazardous Substances Data)

22422-23-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22422-23-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,4,2 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 22422-23:
(7*2)+(6*2)+(5*4)+(4*2)+(3*2)+(2*2)+(1*3)=67
67 % 10 = 7
So 22422-23-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H13ClO/c1-8-3-4-10(7-9(8)2)11(13)5-6-12/h3-4,7H,5-6H2,1-2H3

22422-23-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-chloro-1-(3,4-dimethylphenyl)propan-1-one

1.2 Other means of identification

Product number -
Other names 3-chloro-1-(3,4-dimethyl-phenyl)-propan-1-one

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:22422-23-7 SDS

22422-23-7Relevant articles and documents

Silver-Catalyzed Carbon Dioxide Fixation on Alkynylindenes

Chuang, Po-Yao,Okumura, Akira,Saito, Kodai,Yamada, Tohru

supporting information, (2020/11/13)

The synthesis of polycyclic indene derivatives via silver-catalyzed carbon dioxide fixation on 2-alkynylindene derivatives was achieved by nucleophilic addition of the indenyl anion to carbon dioxide involving carbon-carbon bond formation and subsequent intramolecular cyclization to the alkyne part activated by a silver catalyst. This cascade process could be applied to various substrates to obtain the corresponding products in high yields. The endo/exo selectivity of the cyclization could be controlled by the steric or electronic effect of the substituents on the substrates, and 6-endo-selective cyclization was realized to afford α-pyrone-fused indenes.

TRANSITION METAL COMPOUND AND METHOD FOR PRODUCING OLEFIN POLYMER

-

Paragraph 0072, (2018/11/27)

PROBLEM TO BE SOLVED: To provide a transition metal compound catalyst that makes it possible to synthesize an olefin polymer that is soft and has improved catalytic activity and reduced stereoregularity, and a method for producing an olefin polymer. SOLUTION: The present invention provides a compound represented by formula (IV) (X is a σ-binding or π-binding ligand; Y is a Lewis base; Y may be crosslinked to other Y and X; q is an integer of 1-5 and [(valence of M)-2]; r is an integer of 0-3; R1 and R2 independently represent H or halogen, alkyl or the like; R3-R10 are alkyl groups. M is metal elements of groups 3-10 or lanthanoid series in the periodic table; A1-A4 independently represent a crosslinking group composed of group 14 (C, Si, Ge, Sn)). SELECTED DRAWING: None COPYRIGHT: (C)2018,JPOandINPIT

METALLOCENE COMPLEX AND OLEFIN POLYMERIZATION METHOD

-

Paragraph 0147; 0254, (2015/11/03)

Provided are a metallocene complex that facilitates copolymerization of olefin monomers including propylene at a higher uptake rate of comonomers, i.e., ethylene and α-olefin, manufacture of a rubber component having a higher molecular weight, and manufac

The identification of indacaterol as an ultralong-acting inhaled β2-adrenoceptor agonist

Baur, Fran?ois,Beattie, David,Beer, David,Bentley, David,Bradley, Michelle,Bruce, Ian,Charlton, Steven J.,Cuenoud, Bernard,Ernst, Roland,Fairhurst, Robin A.,Faller, Bernard,Farr, David,Keller, Thomas,Fozard, John R.,Fullerton, Joe,Garman, Sheila,Hatto, Julia,Hayden, Claire,He, Handan,Howes, Colin,Janus, Diana,Jiang, Zhengjin,Lewis, Christine,Loeuillet-Ritzler, Frederique,Moser, Heinz,Reilly, John,Steward, Alan,Sykes, David,Tedaldi, Lauren,Trifilieff, Alexandre,Tweed, Morris,Watson, Simon,Wissler, Elke,Wyss, Daniel

supporting information; experimental part, p. 3675 - 3684 (2010/07/16)

Following a lipophilicity-based hypothesis, an 8-hydroxyquinolinone 2-aminoindan derived series of β2-adrenoceptor agonists have been prepared and evaluated for their potential as inhaled ultralong-acting bronchodilators. Determination of their activities at the human β2-adrenoceptor receptor showed symmetrical substitution of the 2-aminoindan moiety at the 5- and 6-positions delivered the targeted intermediate potency and intrinsic-efficacy profiles relative to a series of clinical reference β2-adrenoceptor agonists. Further assessment with an in vitro superfused electrically stimulated guinea-pig tracheal-strip assay established the onset and duration of action time courses, which could be rationalized by considering the lipophilicity, potency, and intrinsic efficacy of the compounds. From these studies the 5,6-diethylindan analogue indacaterol 1c was shown to possess a unique profile of combining a rapid onset of action with a long duration of action. Further in vivo profiling of 1c supported the long duration of action and a wide therapeutic index following administration to the lung, which led to the compound being selected as a development candidate.

Regioselectivity of acid-catalyzed cyclization of 1-(3,4-dialkylaryl)-3- chloropropan-1-ones to indanones. Comparison of experimental data and results of computer simulation

Ivchenko,Nifant'Ev,Ustynyuk,Ezerskii

experimental part, p. 929 - 935 (2010/10/04)

The acid-catalyzed cyclization of 1-(3,4-dialkylaryl)-3-chloropropan-1-ones to dialkyl-indanones via the intermediate formation of (3,4-dialkylaryl) propenones was studied. This reaction affords isomeric products: 5,6-dialkylindan-1-ones and 4,5-dialkylin

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