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1445899-10-4

2-hydroxy-5-iodophenyl diethylcarbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1445899-10-4 Structure

  • Basic information

    1. Product Name: 2-hydroxy-5-iodophenyl diethylcarbamate
    2. Synonyms: 2-hydroxy-5-iodophenyl diethylcarbamate
    3. CAS NO:1445899-10-4
    4. Molecular Formula:
    5. Molecular Weight: 335.142
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1445899-10-4.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-hydroxy-5-iodophenyl diethylcarbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-hydroxy-5-iodophenyl diethylcarbamate(1445899-10-4)
    11. EPA Substance Registry System: 2-hydroxy-5-iodophenyl diethylcarbamate(1445899-10-4)

  • 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: 1445899-10-4(Hazardous Substances Data)

1445899-10-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1445899-10-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,5,8,9 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1445899-10:
(9*1)+(8*4)+(7*4)+(6*5)+(5*8)+(4*9)+(3*9)+(2*1)+(1*0)=204
204 % 10 = 4
So 1445899-10-4 is a valid CAS Registry Number.

1445899-10-4Downstream Products

1445899-10-4Relevant articles and documents

Ortho-and para-selective ruthenium-catalyzed C(sp2)-H oxygenations of phenol derivatives

Liu, Weiping,Ackermann, Lutz

supporting information, p. 3484 - 3486 (2013/07/26)

Versatile ruthenium catalysts allowed for efficient direct oxygenations of aryl carbamates under remarkably mild reaction conditions. In addition to chelation-assisted C-H activation, the optimized ruthenium catalyst proved amenable to para-selective hydroxylations of anisoles without Lewis basic directing groups.

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