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CAS

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847790-60-7

3β-hydroxy-5-oxo-5,6-seco-[26,26,26,27,27,27]-D6-cholestan-6-al is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 847790-60-7 Structure

  • Basic information

    1. Product Name: 3β-hydroxy-5-oxo-5,6-seco-[26,26,26,27,27,27]-D6-cholestan-6-al
    2. Synonyms: 3β-hydroxy-5-oxo-5,6-seco-[26,26,26,27,27,27]-D6-cholestan-6-al
    3. CAS NO:847790-60-7
    4. Molecular Formula:
    5. Molecular Weight: 424.613
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 847790-60-7.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: 3β-hydroxy-5-oxo-5,6-seco-[26,26,26,27,27,27]-D6-cholestan-6-al(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3β-hydroxy-5-oxo-5,6-seco-[26,26,26,27,27,27]-D6-cholestan-6-al(847790-60-7)
    11. EPA Substance Registry System: 3β-hydroxy-5-oxo-5,6-seco-[26,26,26,27,27,27]-D6-cholestan-6-al(847790-60-7)

  • 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: 847790-60-7(Hazardous Substances Data)

847790-60-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 847790-60-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,7,9 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 847790-60:
(8*8)+(7*4)+(6*7)+(5*7)+(4*9)+(3*0)+(2*6)+(1*0)=217
217 % 10 = 7
So 847790-60-7 is a valid CAS Registry Number.

847790-60-7Downstream Products

847790-60-7Relevant articles and documents

The ratio of cholesterol 5,6-secosterols formed from ozone and singlet oxygen offers insight into the oxidation of cholesterol in vivo

Wentworth, Anita D.,Song, Byeong-Doo,Nieva, Jorge,Shafton, Asher,Tripurenani, Sangeetha,Wentworth Jr., Paul

, p. 3098 - 3100 (2009)

Ongoing efforts to unravel the origins of the cholesterol 5,6-secosterols (1a and 1b) in biological systems have revealed that the two known chemical routes to these oxysterols, ozonolysis of cholesterol (3) and Hock-cleavage of 5-α-hydroperoxycholesterol (4a), are distinguishable based upon the ratio of the hydrazone derivatives (2a and 2b) formed in each case and this ratio offers an insight into the chemical origin of the secosterols in vivo. The Royal Society of Chemistry 2009.

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