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CAS

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1383468-48-1

(R)-isopropyl 2-(2-iodophenoxy)propanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1383468-48-1 Structure

  • Basic information

    1. Product Name: (R)-isopropyl 2-(2-iodophenoxy)propanoate
    2. Synonyms: (R)-isopropyl 2-(2-iodophenoxy)propanoate
    3. CAS NO:1383468-48-1
    4. Molecular Formula:
    5. Molecular Weight: 334.154
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1383468-48-1.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: (R)-isopropyl 2-(2-iodophenoxy)propanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (R)-isopropyl 2-(2-iodophenoxy)propanoate(1383468-48-1)
    11. EPA Substance Registry System: (R)-isopropyl 2-(2-iodophenoxy)propanoate(1383468-48-1)

  • 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: 1383468-48-1(Hazardous Substances Data)

1383468-48-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1383468-48-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,3,4,6 and 8 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1383468-48:
(9*1)+(8*3)+(7*8)+(6*3)+(5*4)+(4*6)+(3*8)+(2*4)+(1*8)=191
191 % 10 = 1
So 1383468-48-1 is a valid CAS Registry Number.

1383468-48-1Downstream Products

1383468-48-1Relevant articles and documents

Chiral aryl iodide-catalyzed enantioselective α-oxidation of ketones

Rodriguez, Arantxa,Moran, Wesley J.

experimental part, p. 1178 - 1182 (2012/06/01)

Several chiral aryl iodides were synthesized and assessed as catalysts in the enantioselective α-oxytosylation of propiophenone and the oxidative cyclization of 5-oxo-5-phenylpentanoic acid to 5-benzoyldihydrofuran-2(3H)-one. The highest enantioselectivit

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