What is the 1-(2,4-dichlorophenyl)cyclopropanecarbonyl chloride?

1-(2,4-dichlorophenyl)cyclopropanecarbonyl chloride is , while it's Molecular Formula is C10H7 Cl3 O. Used in Pharmaceutical Synthesis: 1-(2,4-dichlorophenyl)cyclopropanecarbonyl chloride is used as an intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique chemical structure allows it to be a key component in the development of new medications. Used in Agrochemical Production: In the agrochemical industry, 1-(2,4-dichlorophenyl)cyclopropanecarbonyl chloride is utilized as an intermediate in the production of different agrochemicals, such as pesticides and herbicides. Its reactivity contributes to the formation of active ingredients that help protect crops from pests and diseases. Safety Precautions: Due to its highly toxic and reactive nature, 1-(2,4-dichlorophenyl)cyclopropanecarbonyl chloride requires strict safety measures when being handled or stored. Protective clothing should be worn, and the compound should be manipulated in a well-ventilated area to minimize the risk of respiratory irritation. Additionally, it should be stored in a cool, dry place, away from heat sources and open flames, to prevent the risk of fire or explosion.

What is the 1-(2,4-dichlorophenyl)cyclopropanecarbonyl chloride?

1-(2,4-dichlorophenyl)cyclopropanecarbonyl chloride is , while it's Molecular Formula is C10H7 Cl3 O. Used in Pharmaceutical Synthesis: 1-(2,4-dichlorophenyl)cyclopropanecarbonyl chloride is used as an intermediate in the pharmaceutical industry for the synthesis of various drugs. Its unique chemical structure allows it to be a key component in the development of new medications. Used in Agrochemical Production: In the agrochemical industry, 1-(2,4-dichlorophenyl)cyclopropanecarbonyl chloride is utilized as an intermediate in the production of different agrochemicals, such as pesticides and herbicides. Its reactivity contributes to the formation of active ingredients that help protect crops from pests and diseases. Safety Precautions: Due to its highly toxic and reactive nature, 1-(2,4-dichlorophenyl)cyclopropanecarbonyl chloride requires strict safety measures when being handled or stored. Protective clothing should be worn, and the compound should be manipulated in a well-ventilated area to minimize the risk of respiratory irritation. Additionally, it should be stored in a cool, dry place, away from heat sources and open flames, to prevent the risk of fire or explosion.

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1-(2,4-dichlorophenyl)cyclopropanecarbonyl chloride

Q: What is the CAS number for 1-(2,4-dichlorophenyl)cyclopropanecarbonyl chloride?

The CAS number of 1-(2,4-dichlorophenyl)cyclopropanecarbonyl chloride is 83783-49-7.

Basic Information

CAS No.: 83783-49-7
Purity: 99%

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Details

Manufacturer supply top purity 1-(2,4-dichlorophenyl)cyclopropanecarbonyl chloride 83783-49-7 with ISO standards

Molecular Formula: C10H7 Cl3 O
Molecular Weight: 249.524
Vapor Pressure: 0.000496mmHg at 25°C
Boiling Point: 313.5°C at 760 mmHg
Flash Point: 131.7°C
PSA： 17.07000
Density: 1.504g/cm³
LogP: 3.79040

1-(2,4-dichlorophenyl)cyclopropanecarbonyl chloride(Cas 83783-49-7) Usage

General Description

1-(2,4-dichlorophenyl)cyclopropanecarbonyl chloride is a chemical compound with the molecular formula C10H7Cl2O. It is a derivative of cyclopropane and is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. 1-(2,4-dichlorophenyl)cyclopropanecarbonyl chloride is a reactive and highly toxic substance that can cause severe skin and eye irritation upon contact. It is also a powerful irritant to the respiratory system when inhaled. Therefore, proper safety precautions, such as wearing protective clothing and handling it in a well-ventilated area, should be followed when working with this chemical. Additionally, it should be stored in a cool, dry place away from heat and open flames to prevent the risk of fire or explosion.

InChI:InChI=1/C10H7Cl3O/c11-6-1-2-7(8(12)5-6)10(3-4-10)9(13)14/h1-2,5H,3-4H2

83783-49-7 Relevant articles

Design, synthesis, and analysis of antagonists of GPR55: Piperidine-substituted 1,3,4-oxadiazol-2-ones

Meza-Avi?a, Maria Elena,Lingerfelt, Mary A.,Console-Bram, Linda M.,Gamage, Thomas F.,Sharir, Haleli,Gettys, Kristen E.,Hurst, Dow P.,Kotsikorou, Evangelia,Shore, Derek M.,Caron, Marc G.,Rao, Narasinga,Barak, Larry S.,Abood, Mary E.,Reggio, Patricia H.,Croatt, Mitchell P.

supporting information, p. 1827 - 1830 (2016/12/22)

A series of 1,3,4-oxadiazol-2-ones was s...

Systematic investigation of halogen bonding in protein-ligand interactions

Hardegger, Leo A.,Kuhn, Bernd,Spinnler, Beat,Anselm, Lilli,Ecabert, Robert,Stihle, Martine,Gsell, Bernard,Thoma, Ralf,Diez, Joachim,Benz, Joerg,Plancher, Jean-Marc,Hartmann, Guido,Banner, David W.,Haap, Wolfgang,Diederich, Francois

supporting information; experimental part, p. 314 - 318 (2011/02/28)

Halogen bonding triggers activity: Incre...

Synthesis of β-, γ-, and δ-lactams via Pd(II)-catalyzed C-H activation reactions

Wasa, Masayuki,Yu, Jin-Quan

supporting information; experimental part, p. 14058 - 14059 (2009/03/11)

Pd(II)-catalyzed intramolecular aminatio...

83783-49-7 Process route

: 1-(2,4-dichlorophenyl)cyclopropane-1-carboxylic acid

: 83783-49-7
C₁₀H₇Cl₃O

Conditions

Conditions	Yield
With oxalyl dichloride;
With thionyl chloride; In dichloromethane; at 22 ℃; for 20h; Inert atmosphere;
With thionyl chloride; In dichloromethane; at 50 ℃; for 1h; Inert atmosphere;

: 41661-47-6
piperidin-4-one

: 83783-49-7
C₁₀H₇Cl₃O

: 1-[1-(2,4,-dichlorophenyl)cyclopropanecarbonyl]piperidin-4-one

Conditions

Conditions	Yield
With triethylamine; In tetrahydrofuran; dichloromethane; at 0 - 50 ℃; for 24.25h; Inert atmosphere;	540 mg

83783-49-7 Downstream products

1072810-08-2
C₁₁H₁₁Cl₂NO₂

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