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2-Cyclopropyl-4-(2,6,6-trimethyl-cyclohex-1-enyl)-butan-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 214421-52-0 Structure
  • Basic information

    1. Product Name: 2-Cyclopropyl-4-(2,6,6-trimethyl-cyclohex-1-enyl)-butan-2-ol
    2. Synonyms:
    3. CAS NO:214421-52-0
    4. Molecular Formula:
    5. Molecular Weight: 236.398
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 214421-52-0.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: 2-Cyclopropyl-4-(2,6,6-trimethyl-cyclohex-1-enyl)-butan-2-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Cyclopropyl-4-(2,6,6-trimethyl-cyclohex-1-enyl)-butan-2-ol(214421-52-0)
    11. EPA Substance Registry System: 2-Cyclopropyl-4-(2,6,6-trimethyl-cyclohex-1-enyl)-butan-2-ol(214421-52-0)
  • 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: 214421-52-0(Hazardous Substances Data)

214421-52-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 214421-52-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,4,2 and 1 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 214421-52:
(8*2)+(7*1)+(6*4)+(5*4)+(4*2)+(3*1)+(2*5)+(1*2)=90
90 % 10 = 0
So 214421-52-0 is a valid CAS Registry Number.

214421-52-0Relevant articles and documents

Total synthesis of manoalide

Coombs,Lattmann,Hoffmann

, p. 1367 - 1371 (1998)

Me3Al/AlCl3-mediated hetero-Diels-Alder (HDA) additions of 2-silyloxy-1,3-dienes to formylated butenolide 6 containing a protected hydroxy function afford, in one step, a variety of pyranofuranones including manoalide precursor 16, which is a stable monoprotected seco-manoalide.

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