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Acetamide, N-acetyl-N-(3-nitrophenyl)-, also known as 3-nitro-N-phenylacetamide, is a chemical compound with the molecular formula C10H10N2O4. It is a derivative of acetamide that features an acetyl group and a 3-nitrophenyl group. Acetamide, N-acetyl-N-(3-nitrophenyl)is known for its unique molecular structure and properties, making it a valuable compound in scientific and industrial applications, particularly in pharmaceutical research and development.

3006-36-8

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3006-36-8 Usage

Uses

Used in Pharmaceutical Research and Development:
Acetamide, N-acetyl-N-(3-nitrophenyl)is used as a key intermediate in the synthesis of new drugs. Its pharmacological properties are being studied for potential therapeutic applications, making it an essential component in the development of novel pharmaceuticals.
Used in Organic Synthesis:
Acetamide, N-acetyl-N-(3-nitrophenyl)serves as an important reagent in organic synthesis. Its unique molecular structure allows it to participate in various chemical reactions, contributing to the synthesis of a wide range of organic compounds.
Used in Chemical Product Manufacturing:
Acetamide, N-acetyl-N-(3-nitrophenyl)is also utilized in the manufacturing of various chemical products. Its versatility and reactivity make it a valuable ingredient in the production of different chemical formulations and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 3006-36-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,0 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3006-36:
(6*3)+(5*0)+(4*0)+(3*6)+(2*3)+(1*6)=48
48 % 10 = 8
So 3006-36-8 is a valid CAS Registry Number.

3006-36-8Downstream Products

3006-36-8Relevant academic research and scientific papers

Effect of substituents in the formation of diacetanilides

Ayyangar, Nagaraj R.,Srinivasan, Kumar V.

, p. 1292 - 1296 (2007/10/02)

A number of diacetanilides, including some which have not been reported so far, have been synthesized from the corresponding monoacetyl derivatives and characterized by spectral and elemental analyses.A tlc/fid method for the quantitative estimation of the relative amounts of mono- and diacetyl derivatives has been standardized.Linear correlation of the extent of diacetylation with Hammett ?-values of substituents and basicity constants of monoacetyl derivatives has been established.A plausible mechanism for the diacetylation reaction based on experimental observations has been suggested.An explanation for the anomalous behaviour of acetanilides containing electron-withdrawing substituents in the ortho-position has been put forth.

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