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Benzenemethanol, a-(1,1-dimethyl-3-butenyl)-2-methoxy-5-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 603985-02-0 Structure
  • Basic information

    1. Product Name: Benzenemethanol, a-(1,1-dimethyl-3-butenyl)-2-methoxy-5-methyl-
    2. Synonyms:
    3. CAS NO:603985-02-0
    4. Molecular Formula: C15H22O2
    5. Molecular Weight: 234.338
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 603985-02-0.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: Benzenemethanol, a-(1,1-dimethyl-3-butenyl)-2-methoxy-5-methyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenemethanol, a-(1,1-dimethyl-3-butenyl)-2-methoxy-5-methyl-(603985-02-0)
    11. EPA Substance Registry System: Benzenemethanol, a-(1,1-dimethyl-3-butenyl)-2-methoxy-5-methyl-(603985-02-0)
  • 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: 603985-02-0(Hazardous Substances Data)

603985-02-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 603985-02-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,3,9,8 and 5 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 603985-02:
(8*6)+(7*0)+(6*3)+(5*9)+(4*8)+(3*5)+(2*0)+(1*2)=160
160 % 10 = 0
So 603985-02-0 is a valid CAS Registry Number.

603985-02-0Relevant articles and documents

Total synthesis of (±)-1,13-herbertenediol, (±)-α-herbertenol and (±)-β-herbertenol

Srikrishna,Satyanarayana

, p. 1027 - 1030 (2003)

Total synthesis of α-herbertenol, β-herbertenol and 1,13-herbertenediol, employing a Claisen rearrangement and ring-closing metathesis as key reactions for the generation of the cyclopentane containing vicinal quaternary carbons, has been described.

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