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(1S,6S)-2-Bromo-6-triisopropylsilanyloxy-cyclohexa-2,4-dienol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 219655-88-6 Structure
  • Basic information

    1. Product Name: (1S,6S)-2-Bromo-6-triisopropylsilanyloxy-cyclohexa-2,4-dienol
    2. Synonyms: (1S,6S)-2-Bromo-6-triisopropylsilanyloxy-cyclohexa-2,4-dienol
    3. CAS NO:219655-88-6
    4. Molecular Formula:
    5. Molecular Weight: 347.368
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 219655-88-6.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: (1S,6S)-2-Bromo-6-triisopropylsilanyloxy-cyclohexa-2,4-dienol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1S,6S)-2-Bromo-6-triisopropylsilanyloxy-cyclohexa-2,4-dienol(219655-88-6)
    11. EPA Substance Registry System: (1S,6S)-2-Bromo-6-triisopropylsilanyloxy-cyclohexa-2,4-dienol(219655-88-6)
  • 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: 219655-88-6(Hazardous Substances Data)

219655-88-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 219655-88-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,6,5 and 5 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 219655-88:
(8*2)+(7*1)+(6*9)+(5*6)+(4*5)+(3*5)+(2*8)+(1*8)=166
166 % 10 = 6
So 219655-88-6 is a valid CAS Registry Number.

219655-88-6Relevant articles and documents

The synthesis of (+)-pericosine B

Donohoe, Timothy J.,Blades, Kevin,Helliwell, Madeleine,Waring, Michael J.,Newcombe, Nicholas J.

, p. 8755 - 8758 (1998)

The first synthesis of (+)-pericosine B is described; this takes seven steps and proceeds in 10% overall yield. The key step in our work is a hydrogen-bonding controlled contra-steric dihydroxylation reaction using osmium tetroxide and an amine promoter. The absolute stereochemistry of the natural product was deduced from the known absolute stereochemistry of our starting material and moreover, the relative and absolute stereochemistry of our synthetic material was determined unambiguously from an X-ray crystal structure of an advanced intermediate.

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