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Carbamic acid, 2-propenyl-, phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

40580-72-1

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40580-72-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 40580-72-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,5,8 and 0 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 40580-72:
(7*4)+(6*0)+(5*5)+(4*8)+(3*0)+(2*7)+(1*2)=101
101 % 10 = 1
So 40580-72-1 is a valid CAS Registry Number.

40580-72-1Relevant academic research and scientific papers

Sustainable synthesis routes towards urazole compounds

Vlaminck, Laetitia,Van De Voorde, Babs,Du Prez, Filip E.

supporting information, p. 5659 - 5664 (2017/12/06)

Sustainable synthesis routes towards urazoles, the precursor molecules for triazolinediones, are reported. Not only is the use of isocyanates avoided, but the applied synthetic procedures are also mostly solvent-free, high yielding and performed in an equimolar manner. Two complementary synthesis routes have been developed starting from a wide range of amines, both based on the use of diphenyl carbonate. The first method, which is particularly suitable for the synthesis of bulk urazoles, such as butyl, cyclohexyl or benzyl urazole, is performed in bulk in a one-pot fashion and generally results in yields between 87% and 96%. The second synthesis route, with yields up to 95%, focusses on the implementation of functionalities in the urazole structure and offers the possibility to generate bifunctional urazole compounds.

Manganese dioxide in a new role of Sulfur extrusion in thioamides

Radha Rani,Rahman,Bhalerao

, p. 1953 - 1958 (2007/10/02)

A simple and efficient procedure for the mild conversion of thioamides to amides in good yields using active manganese dioxide is described.

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.

Enzymatic Oxidative Conversion of Thio to Oxo by Baker's Yeast in Thiocarbamates and Thioureas

Kamal, Ahmed,Rao, Maddamsetty V.,Rao, Adari B.

, p. 655 - 656 (2007/10/02)

The enzymatic conversion of aryl allylthiocarbamates and 1-allyl-3-arylthioureas by baker's yeast to the corresponding carbamates and ureas in good yields is described.

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