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  • 1144467-77-5 Structure
  • Basic information

    1. Product Name: C9H11BrO3
    2. Synonyms: C9H11BrO3
    3. CAS NO:1144467-77-5
    4. Molecular Formula:
    5. Molecular Weight: 247.089
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1144467-77-5.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: C9H11BrO3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C9H11BrO3(1144467-77-5)
    11. EPA Substance Registry System: C9H11BrO3(1144467-77-5)
  • 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: 1144467-77-5(Hazardous Substances Data)

1144467-77-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1144467-77-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,4,4,6 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1144467-77:
(9*1)+(8*1)+(7*4)+(6*4)+(5*4)+(4*6)+(3*7)+(2*7)+(1*7)=155
155 % 10 = 5
So 1144467-77-5 is a valid CAS Registry Number.

1144467-77-5Relevant articles and documents

SYNTHESIS OF THE POTENT IMMUNOSUPPRESSANT AGENTS DALESCONOL A AND B

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Page/Page column 7; 61-62, (2011/09/19)

This invention relates to compounds having the structure: wherein bonds α, β, γ, δ, ω, η, χ, ε, κ, and μ are each present or absent, and R1-R18 are various substituents described herein.

Total syntheses of dalesconol A and B

Snyder, Scott A.,Sherwood, Trevor C.,Ross, Audrey G.

supporting information; experimental part, p. 5146 - 5150 (2010/11/04)

(Chemical equation Presented) (Chemical equation Presented) A polycyclic collapse: Use of a carefully designed acyclic intermediate participated in a cascade reaction that formed the entire core of the polyketide-derived dalesconols in a single flask (see scheme). A number of additional and carefully controlled synthetic operations completed an expeditious synthesis of both of these highly bioactive natural products as well as structural congenors.

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