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5829-84-5

2,4-Dichloro-4-phenyl-butyronitrile, also known as 2,4-dichlorophenyl-4-phenylbutyronitrile, is a chemical compound with the molecular formula C14H10Cl2N. It is a white crystalline solid that is soluble in organic solvents. 2,4-Dichloro-4-phenyl-butyronitrile is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of herbicides. Due to its reactivity and potential toxicity, it is important to handle this chemical with care, following proper safety protocols.

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  • 5829-84-5 Structure

  • Basic information

    1. Product Name: 2,4-Dichloro-4-phenyl-butyronitrile
    2. Synonyms:
    3. CAS NO:5829-84-5
    4. Molecular Formula:
    5. Molecular Weight: 214.094
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 5829-84-5.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: 2,4-Dichloro-4-phenyl-butyronitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,4-Dichloro-4-phenyl-butyronitrile(5829-84-5)
    11. EPA Substance Registry System: 2,4-Dichloro-4-phenyl-butyronitrile(5829-84-5)

  • 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: 5829-84-5(Hazardous Substances Data)

5829-84-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5829-84-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,2 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5829-84:
(6*5)+(5*8)+(4*2)+(3*9)+(2*8)+(1*4)=125
125 % 10 = 5
So 5829-84-5 is a valid CAS Registry Number.

5829-84-5Downstream Products

5829-84-5Relevant articles and documents

Atom-transfer radical addition reactions catalyzed by RuCp* complexes: A mechanistic study

Fernandez-Zumel, Mariano A.,Thommes, Katrin,Kiefer, Gregor,Sienkiewicz, Andrzej,Pierzchala, Katarzyna,Severin, Kay

, p. 11601 - 11607 (2009)

Kinetic and spectroscopic analyses were performed to gain information about the mechanism of atomtransfer radical reactions catalyzed by the complexes [RuCl2Cp*(PPh3)] and [RuClCp*(PPh 3)2] (Cp* = pentamethylcyc

Olefin cyclopropanations via sequential atom transfer radical addition-dechlorination reactions

Thommes, Katrin,Severin, Kay

scheme or table, p. 188 - 190 (2011/07/07)

In organic synthesis, cyclopropanation reactions are often performed with Simmons-Smith-type reagents or by transition metal catalyzed reactions of olefins with diazo compounds. A novel method for the synthesis of substituted cyclopropanes is described that is based on a two-step reaction sequence. Olefins are reacted with 1,1'-dichlorides in a Ru-catalyzed atom transfer radical addition (ATRA) process and the resulting 1,3-dichlorides are directly converted into cyclopropanes by reductive coupling with magnesium. This one-pot procedure is applicable to a variety of substrates and can be performed in an inter- or intramolecular fashion. Schweizerische Chemische Gesellschaft.

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