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132905-91-0

4-chlorophenyl isopropylcarbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 132905-91-0 Structure

  • Basic information

    1. Product Name: 4-chlorophenyl isopropylcarbamate
    2. Synonyms: 4-chlorophenyl isopropylcarbamate
    3. CAS NO:132905-91-0
    4. Molecular Formula: C10H12ClNO2
    5. Molecular Weight: 213.66078
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 132905-91-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4-chlorophenyl isopropylcarbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-chlorophenyl isopropylcarbamate(132905-91-0)
    11. EPA Substance Registry System: 4-chlorophenyl isopropylcarbamate(132905-91-0)

  • 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: 132905-91-0(Hazardous Substances Data)

132905-91-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 132905-91-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,9,0 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 132905-91:
(8*1)+(7*3)+(6*2)+(5*9)+(4*0)+(3*5)+(2*9)+(1*1)=120
120 % 10 = 0
So 132905-91-0 is a valid CAS Registry Number.

132905-91-0Downstream Products

132905-91-0Relevant articles and documents

Facile preparation of 2-iodophenyl trifluoromethanesulfonates: Superior aryne precursors

Ganta, Ashok,Snowden, Timothy S.

, p. 2227 - 2231 (2008/02/10)

A comparative study of 3-methoxyaryne precursors revealed 2-iodo-3-methoxyphenyl triflate as the most effective in nonpolar solvent. Use of Hoppe's N-isopropyl carbamate allows for the systematic preparation of a variety of 2-iodophenyl triflates via a directed ortho-lithiation-iodination- decarbamation sequence. These steps are possible without isolation of the intermediate iodophenyl carbamates. Georg Thieme Verlag Stuttgart.

α-Haloalkyl Haloformates and Related Compounds 1. A Convenient Synthesis of Carbamates via Chloromethyl Carbamates

Patonay, Tamas,Patonay-Peli, Erzsebet,Mogyorodi, Ferenc

, p. 2865 - 2885 (2007/10/02)

The preparation of carbamates under mild conditions utilizing a new class of activated carbonates (containing chloromethyl function) is described.

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