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Tert-Butyl (3-oxo-1,2,3,4-tetrahydroquinoxalin-6-yl)carbamate, also known as Boc-protected quinoxaline-6-carboxylic acid, is a chemical compound that serves as a protecting group in organic synthesis. It is a white crystalline solid that is stable under normal conditions and is frequently used as a reagent in the synthesis of various pharmaceuticals, agrochemicals, and other complex organic compounds. The tert-butyl group provides protection for the quinoxaline-6-carboxylic acid, enabling selective reactivity in specific chemical reactions, making it an important intermediate in the production of a wide range of compounds.

1334499-72-7

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1334499-72-7 Usage

Uses

Used in Pharmaceutical Synthesis:
Tert-Butyl (3-oxo-1,2,3,4-tetrahydroquinoxalin-6-yl)carbamate is used as a protecting group for quinoxaline-6-carboxylic acid in the synthesis of pharmaceuticals. The Boc-protecting group allows for selective reactivity in specific chemical reactions, facilitating the synthesis of complex organic compounds and improving the yield and purity of the final product.
Used in Agrochemical Production:
In the agrochemical industry, tert-Butyl (3-oxo-1,2,3,4-tetrahydroquinoxalin-6-yl)carbamate is used as a reagent in the synthesis of various agrochemicals. The protecting group ensures selective reactivity, which is crucial for the production of effective and safe agrochemicals.
Used in Organic Synthesis:
Tert-Butyl (3-oxo-1,2,3,4-tetrahydroquinoxalin-6-yl)carbamate is used as an important intermediate in organic synthesis. Its Boc-protecting group allows for selective reactivity, enabling the synthesis of a wide range of complex organic compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Research and Development:
In research and development, tert-Butyl (3-oxo-1,2,3,4-tetrahydroquinoxalin-6-yl)carbamate is used as a reagent for studying the synthesis and properties of quinoxaline-6-carboxylic acid derivatives. Its Boc-protecting group provides a versatile tool for exploring the reactivity and selectivity of various chemical reactions, contributing to the advancement of organic chemistry and the development of new compounds with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1334499-72-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,4,4,9 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1334499-72:
(9*1)+(8*3)+(7*3)+(6*4)+(5*4)+(4*9)+(3*9)+(2*7)+(1*2)=177
177 % 10 = 7
So 1334499-72-7 is a valid CAS Registry Number.

1334499-72-7Upstream product

1334499-72-7Downstream Products

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