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160024-72-6

(3S)-3-(N-Benzoylamino)-4-methyl-2-pentanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 160024-72-6 Structure

  • Basic information

    1. Product Name: (3S)-3-(N-Benzoylamino)-4-methyl-2-pentanone
    2. Synonyms:
    3. CAS NO:160024-72-6
    4. Molecular Formula:
    5. Molecular Weight: 219.283
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 160024-72-6.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: (3S)-3-(N-Benzoylamino)-4-methyl-2-pentanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3S)-3-(N-Benzoylamino)-4-methyl-2-pentanone(160024-72-6)
    11. EPA Substance Registry System: (3S)-3-(N-Benzoylamino)-4-methyl-2-pentanone(160024-72-6)

  • 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: 160024-72-6(Hazardous Substances Data)

160024-72-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 160024-72-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,0,2 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 160024-72:
(8*1)+(7*6)+(6*0)+(5*0)+(4*2)+(3*4)+(2*7)+(1*2)=86
86 % 10 = 6
So 160024-72-6 is a valid CAS Registry Number.

160024-72-6Downstream Products

160024-72-6Relevant articles and documents

Allylboration of α-Amino Ketones

Pace, R. David,Kabalka, George W.

, p. 4838 - 4844 (1995)

A series of unsaturated α-amino alcohols were prepared via the allylboration of the corresponding N-protected α-amino ketones.The reactions are stereoselective, producing the syn isomers.The diastereoselectivity is not dramatically affected by the electro

Enantiospecific synthesis of 3-pyrrolines: A route to novel polyhydroxylated pyrrolidines

Burley, Ian,Hewson, Alan T.

, p. 7099 - 7102 (2007/10/02)

Enantiomer acetamido ketones are converted by an intramolecular Wittig reaction into enantiopure 3-pyrrolines; the product from (S)-serine provides access to novel polyhydroxylated pyrrolidines.

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