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2,6-diisopropylphenyl 2-bromobutanoate is an organic compound with the molecular formula C18H27BrO2. It is a derivative of phenyl butyrate, featuring a 2-bromobutanoate group attached to a 2,6-diisopropylphenyl moiety. 2,6-diisopropylphenyl 2-bromobutanoate is characterized by its unique structure, which includes two isopropyl groups (C3H7) attached to the phenyl ring at the 2nd and 6th positions, and a 2-bromobutanoate group (CH3CHBrCH2COO-) attached to the phenyl ring. The presence of the bromine atom in the 2-bromobutanoate group imparts specific chemical properties to the molecule, such as increased reactivity and potential for substitution reactions. 2,6-diisopropylphenyl 2-bromobutanoate may be used in various chemical synthesis processes, particularly in the pharmaceutical and agrochemical industries, due to its unique structure and reactivity.

1440-80-8

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1440-80-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1440-80-8 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, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1440-80:
(6*1)+(5*4)+(4*4)+(3*0)+(2*8)+(1*0)=58
58 % 10 = 8
So 1440-80-8 is a valid CAS Registry Number.

1440-80-8Relevant 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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