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CAS

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1203905-07-0

[2-(6-allyloxy-2-bromo-3-hydroxyphenyl)ethyl]carbamic acid tert-butyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1203905-07-0 Structure

  • Basic information

    1. Product Name: [2-(6-allyloxy-2-bromo-3-hydroxyphenyl)ethyl]carbamic acid tert-butyl ester
    2. Synonyms: [2-(6-allyloxy-2-bromo-3-hydroxyphenyl)ethyl]carbamic acid tert-butyl ester
    3. CAS NO:1203905-07-0
    4. Molecular Formula:
    5. Molecular Weight: 372.259
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1203905-07-0.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: [2-(6-allyloxy-2-bromo-3-hydroxyphenyl)ethyl]carbamic acid tert-butyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: [2-(6-allyloxy-2-bromo-3-hydroxyphenyl)ethyl]carbamic acid tert-butyl ester(1203905-07-0)
    11. EPA Substance Registry System: [2-(6-allyloxy-2-bromo-3-hydroxyphenyl)ethyl]carbamic acid tert-butyl ester(1203905-07-0)

  • 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: 1203905-07-0(Hazardous Substances Data)

1203905-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1203905-07-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,3,9,0 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1203905-07:
(9*1)+(8*2)+(7*0)+(6*3)+(5*9)+(4*0)+(3*5)+(2*0)+(1*7)=110
110 % 10 = 0
So 1203905-07-0 is a valid CAS Registry Number.

1203905-07-0Relevant articles and documents

The coumarin→indole transformation - A method for preparing 4-halo-5-hydroxyindoles from coumarins

Stoffman, Elia J. L.,Clive, Derrick. L. J.

, p. 4862 - 4870 (2009)

Readily accessible 3-alkoxycarbonyl-6-hydroxy-5-halocoumarins can be converted into 4-halo-5-hydroxyindoles by a sequence whose essential steps are conjugate reduction or conjugate addition, decarboxylation, lactone opening with ammonia, phenolic oxygen p

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