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Ethyl 6-bromo-4-oxo-3,4-dihydro-2H-benzo[e][1,3]oxazine-2-carboxylate is a chemical compound characterized by its molecular formula C11H10BrNO4. It is an organic ester that features a benzooxazine ring and a carboxylate functional group. Ethyl 6-bromo-4-oxo-3,4-dihydro-2H-benzo[e][1,3]oxazine-2-carboxylate is recognized for its potential in the synthesis of pharmaceuticals and organic compounds, as well as its utility as a reagent in organic chemistry reactions. The bromine atom in its structure contributes to its value as a building block for more complex organic molecules, while the oxazine ring structure suggests its potential in the development of novel drugs and bioactive compounds.

30482-66-7

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30482-66-7 Usage

Uses

Used in Pharmaceutical Synthesis:
Ethyl 6-bromo-4-oxo-3,4-dihydro-2H-benzo[e][1,3]oxazine-2-carboxylate is used as a key intermediate in the synthesis of pharmaceuticals for its ability to be incorporated into more complex molecular structures, enhancing the development of new medications.
Used in Organic Chemistry as a Reagent:
In the realm of organic chemistry, Ethyl 6-bromo-4-oxo-3,4-dihydro-2H-benzo[e][1,3]oxazine-2-carboxylate serves as a reagent, facilitating various chemical reactions that are essential for the creation of a wide range of organic compounds.
Used in the Preparation of Complex Organic Molecules:
The presence of the bromine atom in Ethyl 6-bromo-4-oxo-3,4-dihydro-2H-benzo[e][1,3]oxazine-2-carboxylate makes it a useful building block for the preparation of complex organic molecules, which can be vital in advancing material science and chemical research.
Used in Drug Development:
The oxazine ring structure of Ethyl 6-bromo-4-oxo-3,4-dihydro-2H-benzo[e][1,3]oxazine-2-carboxylate makes it potentially useful in the development of novel drugs, suggesting its application in medicinal chemistry for the creation of new bioactive compounds with therapeutic potential.
Used in Chemical Research:
Ethyl 6-bromo-4-oxo-3,4-dihydro-2H-benzo[e][1,3]oxazine-2-carboxylate is utilized in chemical research to explore its properties and reactivity, contributing to the understanding of organic ester chemistry and its implications in various chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 30482-66-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,4,8 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 30482-66:
(7*3)+(6*0)+(5*4)+(4*8)+(3*2)+(2*6)+(1*6)=97
97 % 10 = 7
So 30482-66-7 is a valid CAS Registry Number.
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