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CAS

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74708-32-0

(1S,2S,R)-cis-1-(2-Hydroxycyclohexyl)methyl N-<1-(1-Naphthyl)-ethyl>amide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 74708-32-0 Structure

  • Basic information

    1. Product Name: (1S,2S,R)-cis-1-(2-Hydroxycyclohexyl)methyl N-<1-(1-Naphthyl)-ethyl>amide
    2. Synonyms:
    3. CAS NO:74708-32-0
    4. Molecular Formula:
    5. Molecular Weight: 311.424
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 74708-32-0.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: (1S,2S,R)-cis-1-(2-Hydroxycyclohexyl)methyl N-<1-(1-Naphthyl)-ethyl>amide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1S,2S,R)-cis-1-(2-Hydroxycyclohexyl)methyl N-<1-(1-Naphthyl)-ethyl>amide(74708-32-0)
    11. EPA Substance Registry System: (1S,2S,R)-cis-1-(2-Hydroxycyclohexyl)methyl N-<1-(1-Naphthyl)-ethyl>amide(74708-32-0)

  • 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: 74708-32-0(Hazardous Substances Data)

74708-32-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74708-32-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,7,0 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 74708-32:
(7*7)+(6*4)+(5*7)+(4*0)+(3*8)+(2*3)+(1*2)=140
140 % 10 = 0
So 74708-32-0 is a valid CAS Registry Number.

74708-32-0Downstream Products

74708-32-0Relevant articles and documents

Enantiomerically Pure Lactones. 2. Approaches to Cis or Trans Multicyclic Lactones

Pirkle, William H.,Adams, Paul E.

, p. 4111 - 4117 (2007/10/02)

Enantiomerically pure bicyclic lactones 1-3 and tricyclic lactones 4 and 5 have been prepared by either of two procedures, each hinging upon the liquid chromatographic seperation of rationally selected diastereomeric derivatives.After seperation, the diastereomers are converted by a simple high-yield reaction sequence to the enantiomeric multiring lactones, none of which has been previously reported in optically active form. The relative strengths and weaknesses of each approach are discussed.Lactones 4 and 5 were α-methylated, these derivatives being suitable for the determination of enantiomeric purity and absolute configuration using the chiral solvating agent (S)-(+)-2,2,2-trifluoro-1-(9-anthryl)ethanol.

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