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150547-30-1

(R)-2-hydroxy-4-octanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 150547-30-1 Structure

  • Basic information

    1. Product Name: (R)-2-hydroxy-4-octanone
    2. Synonyms: (R)-2-hydroxy-4-octanone
    3. CAS NO:150547-30-1
    4. Molecular Formula:
    5. Molecular Weight: 144.214
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 150547-30-1.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: (R)-2-hydroxy-4-octanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-2-hydroxy-4-octanone(150547-30-1)
    11. EPA Substance Registry System: (R)-2-hydroxy-4-octanone(150547-30-1)

  • 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: 150547-30-1(Hazardous Substances Data)

150547-30-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 150547-30-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,0,5,4 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 150547-30:
(8*1)+(7*5)+(6*0)+(5*5)+(4*4)+(3*7)+(2*3)+(1*0)=111
111 % 10 = 1
So 150547-30-1 is a valid CAS Registry Number.

150547-30-1Upstream product

150547-30-1Downstream Products

150547-30-1Relevant articles and documents

Dienes as Chiral Templates: Easy Access to Pure (2S,3S,4R)-4-Hydroxy-2,3-epoxycyclohex-5-en-1-one

Mauvais, Antony,Winterfeldt, Ekkehard

, p. 5817 - 5822 (1993)

The title compound 6 was obtained stereospecifically through a concise sequence including a Diels-Alder reaction with the chiral diene 2 and the retro reaction.The Favorskii rearrangement starting from the intermediate epoxide 4 was found to be regioselec

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