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CAS

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122922-55-8

(3R,4R)-3-((R)-1-hydroxy-5-methylhexyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 122922-55-8 Structure

  • Basic information

    1. Product Name: (3R,4R)-3-((R)-1-hydroxy-5-methylhexyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one
    2. Synonyms:
    3. CAS NO:122922-55-8
    4. Molecular Formula:
    5. Molecular Weight: 230.304
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 122922-55-8.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: (3R,4R)-3-((R)-1-hydroxy-5-methylhexyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: (3R,4R)-3-((R)-1-hydroxy-5-methylhexyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one(122922-55-8)
    11. EPA Substance Registry System: (3R,4R)-3-((R)-1-hydroxy-5-methylhexyl)-4-(hydroxymethyl)dihydrofuran-2(3H)-one(122922-55-8)

  • 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: 122922-55-8(Hazardous Substances Data)

122922-55-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122922-55-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,9,2 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 122922-55:
(8*1)+(7*2)+(6*2)+(5*9)+(4*2)+(3*2)+(2*5)+(1*5)=108
108 % 10 = 8
So 122922-55-8 is a valid CAS Registry Number.

122922-55-8Relevant articles and documents

Stereochemistry of butyrolactone autoregulators from streptomyces

Sakuda, Shohei,Yamada, Yasuhiro

, p. 1817 - 1820 (1991)

Stereochemistry of virginiae butanolide A 3 was elucidated by its chemical conversion to the acetal 14, establishing also the structures of other related compounds.

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