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362519-24-2

(S)-(+)-hexahydromandelamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 362519-24-2 Structure

  • Basic information

    1. Product Name: (S)-(+)-hexahydromandelamide
    2. Synonyms: (S)-(+)-hexahydromandelamide
    3. CAS NO:362519-24-2
    4. Molecular Formula:
    5. Molecular Weight: 157.213
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 362519-24-2.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: (S)-(+)-hexahydromandelamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-(+)-hexahydromandelamide(362519-24-2)
    11. EPA Substance Registry System: (S)-(+)-hexahydromandelamide(362519-24-2)

  • 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: 362519-24-2(Hazardous Substances Data)

362519-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 362519-24-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,2,5,1 and 9 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 362519-24:
(8*3)+(7*6)+(6*2)+(5*5)+(4*1)+(3*9)+(2*2)+(1*4)=142
142 % 10 = 2
So 362519-24-2 is a valid CAS Registry Number.

362519-24-2Relevant articles and documents

1,1′-Binaphthylazepine-based ligands for asymmetric catalysis. Part 1: Preparation and characterization of some new aminoalcohols and diamines

Mecca, Tommaso,Superchi, Stefano,Giorgio, Egidio,Rosini, Carlo

, p. 1225 - 1233 (2007/10/03)

Starting from (S)-1,1′-binaphthol, a series of ten novel enantiopure 1,1′-binaphthylazepine-based aminoalcohols and diamines 1a-1j were efficiently prepared and fully characterized. These derivatives, having either only an atropisomeric bridged-binaphthyl backbone or an additional stereogenic carbon center, can be interesting ligands for asymmetric catalysis.

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