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433335-00-3

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433335-00-3 Usage

General Description

The chemicals "N-Boc-(p-tosyl)methanamine, tert-Butyl tosylmethylcarbamate, (Toluene-4-sulfonylmethyl)carbamic acid, tert-butyl ester" are all compounds containing tosyl groups and carbamate groups. N-Boc-(p-tosyl)methanamine is a derivative of p-toluenesulfonamide and is commonly used as a protecting group in organic synthesis. tert-Butyl tosylmethylcarbamate is an intermediate compound used in the synthesis of various pharmaceuticals and agrochemicals. (Toluene-4-sulfonylmethyl)carbamic acid, tert-butyl ester is a carbamate compound that can be used as a reagent in organic synthesis for the preparation of various compounds. These chemicals are important intermediates with a wide range of applications in the manufacturing of pharmaceuticals, agrochemicals, and other organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 433335-00-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,3,3,3 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 433335-00:
(8*4)+(7*3)+(6*3)+(5*3)+(4*3)+(3*5)+(2*0)+(1*0)=113
113 % 10 = 3
So 433335-00-3 is a valid CAS Registry Number.

433335-00-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
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  • Aldrich

  • (687006)  N-Boc-(tosyl)methylamine  97%

  • 433335-00-3

  • 687006-1G

  • 600.21CNY

  • Detail
  • Aldrich

  • (687006)  N-Boc-(tosyl)methylamine  97%

  • 433335-00-3

  • 687006-5G

  • 1,794.78CNY

  • Detail

433335-00-3Relevant articles and documents

An Efficient Direct Access to Carbamates from Alcohols and TosMIC Mediated by Iodine in DMSO

Pogaku, Naresh,Krishna, Palakodety Radha,Prapurna, Y. Lakshmi

supporting information, p. 2039 - 2042 (2018/09/18)

A new approach for the synthesis of carbamates from alcohols and TosMIC promoted by iodine/DMSO system is reported. This method offers a one-step, direct and practical strategy for the rapid construction of carbamates under mild conditions. The reaction proceeds via sequential oxidation of isocyanide to isocyanate and nucleophilic addition of alcohols to isocyanate to afford the carbamates in high yields.

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