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1582273-36-6

isopropyl (4-(tert-butyl)phenyl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1582273-36-6 Structure

  • Basic information

    1. Product Name: isopropyl (4-(tert-butyl)phenyl)carbamate
    2. Synonyms:
    3. CAS NO:1582273-36-6
    4. Molecular Formula:
    5. Molecular Weight: 235.326
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1582273-36-6.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: isopropyl (4-(tert-butyl)phenyl)carbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: isopropyl (4-(tert-butyl)phenyl)carbamate(1582273-36-6)
    11. EPA Substance Registry System: isopropyl (4-(tert-butyl)phenyl)carbamate(1582273-36-6)

  • 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: 1582273-36-6(Hazardous Substances Data)

1582273-36-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1582273-36-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,2,2,7 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1582273-36:
(9*1)+(8*5)+(7*8)+(6*2)+(5*2)+(4*7)+(3*3)+(2*3)+(1*6)=176
176 % 10 = 6
So 1582273-36-6 is a valid CAS Registry Number.

1582273-36-6Downstream Products

1582273-36-6Relevant articles and documents

Metal free oxidative coupling of aryl formamides with alcohols for the synthesis of carbamates

Reddy, N. Veera,Prasad, K. Rajendra,Reddy, P. Sudhir,Lakshmi Kantam,Reddy, K. Rajender

, p. 2172 - 2175 (2014)

A direct transformation of N-aryl formamides to the corresponding carbamates via the formation of isocyanate intermediates is achieved in good yields using hypervalent iodine as an oxidant. This journal is

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