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CAS

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214629-64-8

tert-Butyl-[(1S,2R)-2-(2-methoxy-4-methyl-phenyl)-cyclohex-3-enyloxy]-dimethyl-silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 214629-64-8 Structure

  • Basic information

    1. Product Name: tert-Butyl-[(1S,2R)-2-(2-methoxy-4-methyl-phenyl)-cyclohex-3-enyloxy]-dimethyl-silane
    2. Synonyms: tert-Butyl-[(1S,2R)-2-(2-methoxy-4-methyl-phenyl)-cyclohex-3-enyloxy]-dimethyl-silane
    3. CAS NO:214629-64-8
    4. Molecular Formula:
    5. Molecular Weight: 332.558
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 214629-64-8.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: tert-Butyl-[(1S,2R)-2-(2-methoxy-4-methyl-phenyl)-cyclohex-3-enyloxy]-dimethyl-silane(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-Butyl-[(1S,2R)-2-(2-methoxy-4-methyl-phenyl)-cyclohex-3-enyloxy]-dimethyl-silane(214629-64-8)
    11. EPA Substance Registry System: tert-Butyl-[(1S,2R)-2-(2-methoxy-4-methyl-phenyl)-cyclohex-3-enyloxy]-dimethyl-silane(214629-64-8)

  • 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: 214629-64-8(Hazardous Substances Data)

214629-64-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 214629-64-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,6,2 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 214629-64:
(8*2)+(7*1)+(6*4)+(5*6)+(4*2)+(3*9)+(2*6)+(1*4)=128
128 % 10 = 8
So 214629-64-8 is a valid CAS Registry Number.

214629-64-8Relevant articles and documents

Enantioselective construction and utilization of 2-(cyclohex-2-enyl)phenols

Konno, Hiroyuki,Ogasawara, Kunio

, p. 1004 - 1006 (2007/10/03)

Enantioselective construction of 2-(cyclohex-2-enyl)phenols from chiral equivalents of cyclohex-2-enols has been investigated by employing a concurrent retro-Diels-Alder reaction and Claisen rearrangement protocol. Utilizing the enantiomerically pure product obtained, the first enantiocontrolled synthesis of a phenolic natural sesquiterpene (+)-curcudiol, isolated from the marine sponge Didiscus flavus, has been demonstrated.

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