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218129-86-3

3-trityloxymethyl-cyclohex-2-enol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 218129-86-3 Structure

  • Basic information

    1. Product Name: 3-trityloxymethyl-cyclohex-2-enol
    2. Synonyms: 3-trityloxymethyl-cyclohex-2-enol
    3. CAS NO:218129-86-3
    4. Molecular Formula:
    5. Molecular Weight: 370.491
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 218129-86-3.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: 3-trityloxymethyl-cyclohex-2-enol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-trityloxymethyl-cyclohex-2-enol(218129-86-3)
    11. EPA Substance Registry System: 3-trityloxymethyl-cyclohex-2-enol(218129-86-3)

  • 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: 218129-86-3(Hazardous Substances Data)

218129-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 218129-86-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,8,1,2 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 218129-86:
(8*2)+(7*1)+(6*8)+(5*1)+(4*2)+(3*9)+(2*8)+(1*6)=133
133 % 10 = 3
So 218129-86-3 is a valid CAS Registry Number.

218129-86-3Relevant articles and documents

Studies on the substituted 3-aminopropan-1-ol motif of lycoctonine class norditerpenid alkaloids: A novel route to 3-hydroxymethylcyclohex-2-enone

Doisy, Xavier,Blagbrough, Ian S.,Thomas, Noel F.,Potter, Barry V. L.

, p. 8525 - 8528 (1998)

Pursuing our interest in methyllcaconitine (MLA), we have designed a synthetic route to substituted ring-A of lycoctonine class norditerpenoid alkaloids. A novel synthesis of 3-hydroxymethylcyclohex-2-enone has been achieved starting from cyclohex-2-enone. Key reactions are: 1,2-addition of 1,3-dithiane followed by allylic rearrangement, 1,4-hydrocyanation, Wittig reaction and conversion into the substituted N-ethyl-3-aminopropan-1-ol motif of these neopentyl-like alcohols.

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