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CAS

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403483-76-1

2-Cyclohexen-1-one, 6-[(2E)-3-(dimethylphenylsilyl)-2-butenyl]-3,5,5-trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 403483-76-1 Structure

  • Basic information

    1. Product Name: 2-Cyclohexen-1-one, 6-[(2E)-3-(dimethylphenylsilyl)-2-butenyl]-3,5,5-trimethyl-
    2. Synonyms:
    3. CAS NO:403483-76-1
    4. Molecular Formula: C21H30OSi
    5. Molecular Weight: 326.554
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 403483-76-1.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-Cyclohexen-1-one, 6-[(2E)-3-(dimethylphenylsilyl)-2-butenyl]-3,5,5-trimethyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Cyclohexen-1-one, 6-[(2E)-3-(dimethylphenylsilyl)-2-butenyl]-3,5,5-trimethyl-(403483-76-1)
    11. EPA Substance Registry System: 2-Cyclohexen-1-one, 6-[(2E)-3-(dimethylphenylsilyl)-2-butenyl]-3,5,5-trimethyl-(403483-76-1)

  • 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: 403483-76-1(Hazardous Substances Data)

403483-76-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 403483-76-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,3,4,8 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 403483-76:
(8*4)+(7*0)+(6*3)+(5*4)+(4*8)+(3*3)+(2*7)+(1*6)=131
131 % 10 = 1
So 403483-76-1 is a valid CAS Registry Number.

403483-76-1Relevant articles and documents

A novel extension of the Stork-Jung vinylsilane Robinson annelation procedure for the introduction of the cyclohexene of guanacastepene

Snider, Barry B,Shi, Bo

, p. 9123 - 9126 (2007/10/03)

A new annelation procedure has been developed in a model system to introduce the cyclohexene ring of guanacastepene. Cyclohexenone 16 is prepared by sequential methylation and alkylation with allylic iodide 15. One-pot epoxidation, protodesilylation and hydrolysis of the THP forms dione 19, which cyclizes with NaOMe to 24 in 57% overall yield. Reduction, Mitsunobu inversion, and selective oxidation of the primary alcohol forms model 29. Phenyldimethylsilyl allylic iodide 36 is easier to make and more stable than trimethylsilyl allylic iodide 6 used by Stork.

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