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943154-99-2

(S)-3-(benzyloxy)-3-methylhex-5-en-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 943154-99-2 Structure

  • Basic information

    1. Product Name: (S)-3-(benzyloxy)-3-methylhex-5-en-1-ol
    2. Synonyms: (S)-3-(benzyloxy)-3-methylhex-5-en-1-ol
    3. CAS NO:943154-99-2
    4. Molecular Formula:
    5. Molecular Weight: 220.312
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 943154-99-2.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: (S)-3-(benzyloxy)-3-methylhex-5-en-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-3-(benzyloxy)-3-methylhex-5-en-1-ol(943154-99-2)
    11. EPA Substance Registry System: (S)-3-(benzyloxy)-3-methylhex-5-en-1-ol(943154-99-2)

  • 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: 943154-99-2(Hazardous Substances Data)

943154-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 943154-99-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,1,5 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 943154-99:
(8*9)+(7*4)+(6*3)+(5*1)+(4*5)+(3*4)+(2*9)+(1*9)=182
182 % 10 = 2
So 943154-99-2 is a valid CAS Registry Number.

943154-99-2Relevant articles and documents

An efficient asymmetric route to tertiary carbinols: Synthesis of (R)-mevalonolactone

Roy,Sharma,Dhotare,Vichare,Chattopadhyay,Chattopadhyay

, p. 1082 - 1090 (2008/02/02)

An efficient strategy for the asymmetric construction of tertiary carbinols has been devised using cyclohexylideneglyceraldehyde as a chiral template. This involves (a) addition of a Grignard reagent (R1MgX) to cyclohexylideneglyceraldehyde, fo

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