Cas no 127082-54-6 (Benzamide, 2-(benzoylamino)-N-methyl-)

Benzamide, 2-(benzoylamino)-N-methyl-, is a specialized organic compound featuring a benzamide core substituted with a benzoylamino group at the 2-position and an N-methyl moiety. This structure imparts unique reactivity and functional properties, making it valuable in synthetic chemistry and pharmaceutical research. Its dual amide functionality enhances stability and potential for hydrogen bonding, which can be leveraged in molecular design or as an intermediate in heterocyclic synthesis. The compound's well-defined aromatic and amide groups also facilitate applications in crystallography or as a reference standard. High purity grades ensure consistency in research and industrial processes, supporting precise experimental outcomes.
Benzamide, 2-(benzoylamino)-N-methyl- structure
127082-54-6 structure
Product Name:Benzamide, 2-(benzoylamino)-N-methyl-
CAS No:127082-54-6
MF:C15H14N2O2
MW:254.283863544464
CID:1221272
PubChem ID:12323674
Update Time:2025-05-22

Benzamide, 2-(benzoylamino)-N-methyl- Chemical and Physical Properties

Names and Identifiers

    • Benzamide, 2-(benzoylamino)-N-methyl-
    • 2-(benzoylamino)-N-methylbenzamide
    • 2-Benzamido-N-methylbenzamide
    • AKOS000500024
    • AN-329/40096857
    • STL062041
    • CCG-287719
    • 127082-54-6
    • N-methyl-2-[(phenylcarbonyl)amino]benzamide
    • CS-0359073
    • MDL: MFCD00433994
    • Inchi: 1S/C15H14N2O2/c1-16-15(19)12-9-5-6-10-13(12)17-14(18)11-7-3-2-4-8-11/h2-10H,1H3,(H,16,19)(H,17,18)
    • InChI Key: FQNPBZCBLVTENV-UHFFFAOYSA-N
    • SMILES: O=C(C1C=CC=CC=1)NC1C=CC=CC=1C(NC)=O

Computed Properties

  • Exact Mass: 254.10562
  • Monoisotopic Mass: 254.105527694g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 19
  • Rotatable Bond Count: 5
  • Complexity: 324
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.9
  • Topological Polar Surface Area: 58.2?2

Experimental Properties

  • PSA: 58.2

Benzamide, 2-(benzoylamino)-N-methyl- Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.
1429743-1g
2-Benzamido-N-methylbenzamide
127082-54-6 98%
1g
¥19051.00 2024-08-09
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.
1429743-5g
2-Benzamido-N-methylbenzamide
127082-54-6 98%
5g
¥22500.00 2024-08-09
SHANG HAI HAO HONG Biomedical Technology Co., Ltd.
1429743-10g
2-Benzamido-N-methylbenzamide
127082-54-6 98%
10g
¥35857.00 2024-08-09

Additional information on Benzamide, 2-(benzoylamino)-N-methyl-

Benzamide, 2-(benzoylamino)-N-methyl-: A Comprehensive Overview

Benzamide, 2-(benzoylamino)-N-methyl- (CAS No. 127082-54-6) is a versatile organic compound with significant applications in various fields of chemistry and materials science. This compound, often referred to as Benzamide, 2-(benzoylamino)-N-methyl or N-methyl-2-(benzoylamino)benzamide, has garnered attention due to its unique chemical properties and potential uses in drug development, polymer synthesis, and advanced materials. Recent studies have highlighted its role in enhancing the performance of organic semiconductors and its ability to act as a building block in complex molecular architectures.

The chemical structure of Benzamide, 2-(benzoylamino)-N-methyl- consists of a benzene ring substituted with an amide group at the second position. The amide group is further modified with a methyl substituent on the nitrogen atom, which imparts unique electronic and steric properties to the molecule. This structure allows for strong intermolecular interactions, making it suitable for applications in crystal engineering and supramolecular chemistry.

Recent research has focused on the synthesis and characterization of this compound. Scientists have developed efficient synthetic routes using coupling reactions and amidation techniques, ensuring high yields and purity. The compound's stability under various conditions has been thoroughly investigated, revealing its resistance to thermal degradation and chemical corrosion, which are critical factors for industrial applications.

In terms of physical properties, Benzamide, 2-(benzoylamino)-N-methyl- exhibits a high melting point due to its strong intermolecular hydrogen bonding network. Its solubility in organic solvents makes it ideal for use in solution-based processes, such as polymerization reactions and thin-film deposition. Additionally, the compound's optical properties have been explored for potential applications in optoelectronic devices.

The application of Benzamide, 2-(benzoylamino)-N-methyl- spans multiple domains. In the pharmaceutical industry, it serves as a key intermediate in the synthesis of bioactive compounds targeting various diseases. Recent studies have demonstrated its role in inhibiting specific enzymes associated with neurodegenerative disorders, highlighting its potential as a lead compound for drug development.

In materials science, this compound has been utilized as a precursor for synthesizing advanced polymers and hybrid materials. Its ability to form stable co-crystals with other organic molecules has opened new avenues for designing functional materials with tailored properties. Researchers have also explored its use in creating self-healing polymers, which can autonomously repair damage under specific conditions.

Moreover, Benzamide, 2-(benzoylamino)-N-methyl- has shown promise in the field of green chemistry. Its involvement in catalytic processes that reduce environmental impact has made it a valuable tool for sustainable chemical manufacturing. Recent advancements include its use as a catalyst in asymmetric synthesis reactions, enabling the production of enantiomerically pure compounds with high efficiency.

The toxicological profile of this compound has also been assessed to ensure its safety for industrial and medical applications. Studies indicate that it exhibits low toxicity when handled under standard conditions, making it suitable for large-scale production processes.

Looking ahead, the future of Benzamide, 2-(benzoylamino)-N-methyl- seems bright. Ongoing research is focused on expanding its applications in nanotechnology and biotechnology. Its integration into nanomaterials could lead to breakthroughs in areas such as drug delivery systems and biosensors.

In conclusion, Benzamide, 2-(benzoylamino)-N-methyl- (CAS No. 127082-54-6) is a multifaceted compound with immense potential across diverse scientific disciplines. Its unique chemical properties, coupled with recent advancements in synthesis and application techniques, position it as a key player in modern chemical research and development.

Recommended suppliers
TAIXING JOXIN BIO-TEC CO.,LTD.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
TAIXING JOXIN BIO-TEC CO.,LTD.
Inner Mongolia Xinhong Biological Technology Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Inner Mongolia Xinhong Biological Technology Co., Ltd
Jinta Yudi Pharmaceutical Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Jinta Yudi Pharmaceutical Technology Co., Ltd.
Suzhou Senfeida Chemical Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Suzhou Senfeida Chemical Co., Ltd
Wuhan ChemNorm Biotech Co.,Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
Wuhan ChemNorm Biotech Co.,Ltd.