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2,2-dimethyl-3-phenylbutanal is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 61866-24-8 Structure
  • Basic information

    1. Product Name: 2,2-dimethyl-3-phenylbutanal
    2. Synonyms: 2,2-dimethyl-3-phenylbutanal
    3. CAS NO:61866-24-8
    4. Molecular Formula:
    5. Molecular Weight: 176.258
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 61866-24-8.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: 2,2-dimethyl-3-phenylbutanal(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,2-dimethyl-3-phenylbutanal(61866-24-8)
    11. EPA Substance Registry System: 2,2-dimethyl-3-phenylbutanal(61866-24-8)
  • 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: 61866-24-8(Hazardous Substances Data)

61866-24-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61866-24-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,8,6 and 6 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 61866-24:
(7*6)+(6*1)+(5*8)+(4*6)+(3*6)+(2*2)+(1*4)=138
138 % 10 = 8
So 61866-24-8 is a valid CAS Registry Number.

61866-24-8Downstream Products

61866-24-8Relevant articles and documents

Indium-catalyzed coupling reaction between silyl enolates and alkyl chlorides or alkyl ethers

Nishimoto, Yoshihiro,Saito, Takahiro,Yasuda, Makoto,Baba, Akio

experimental part, p. 5462 - 5471 (2009/12/01)

The coupling reactions of alkyl chlorides with silyl enolates catalyzed by InBr3, and the coupling reactions of alkyl ethers with silyl enolates catalyzed by the combined Lewis acid of InBr3/Me3SiBr are described. In both reaction systems, various types of silyl enolates were used to give corresponding α-alkylated esters, ketones, carboxylic acids, amides, thioesters, and aldehydes.

Coupling reaction of alkyl chlorides with silyl enolates catalyzed by indium trihalide

Nishimoto, Yoshihiro,Yasuda, Makoto,Baba, Akio

, p. 4931 - 4934 (2008/03/27)

Indium(III) halide catalyzed not only the coupling of alkyl chlorides with silyl enolates derived from esters, ketones, and aldehydes to give a variety of α-alkylated carbonyl compounds but also one-pot, three-component reactions of aldehyde enolate, alkyl chloride, and allylsilane or alkynylsilane.

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