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2,6-diisopropylphenyl 2-bromopropanoate is an organic compound with the molecular formula C15H21BrO2. It is a derivative of phenylpropanoic acid, featuring a 2-bromopropanoate group attached to the 2,6-diisopropylphenyl moiety. 2,6-diisopropylphenyl 2-bromopropanoate is characterized by its unique structure, which includes two isopropyl groups (C3H7) at the 2nd and 6th positions of the phenyl ring, and a 2-bromopropanoate group (CH3CHBrCOO-) at the para position. The presence of the bromine atom in the 2-bromopropanoate group imparts specific chemical properties and reactivity to the molecule. 2,6-diisopropylphenyl 2-bromopropanoate may have potential applications in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals, where its unique structure could be exploited for specific functional groups or reactivity patterns.

1440-79-5

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1440-79-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1440-79-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,4 and 0 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1440-79:
(6*1)+(5*4)+(4*4)+(3*0)+(2*7)+(1*9)=65
65 % 10 = 5
So 1440-79-5 is a valid CAS Registry Number.

1440-79-5Relevant academic research and scientific papers

A diastereo- and enantioselective synthesis of α-substituted syn-α,β-diamino acids

Singh, Anand,Johnston, Jeffrey N.

, p. 5866 - 5867 (2008/09/19)

Highly diastereo- and enantioselective additions of substituted α-nitroesters to imines have been developed. High diastereoselection relies on the finding that the combination of chiral proton catalyst 2b and α-nitro aryl esters bearing 2,6-disubstitution

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