Oxamide - ≥98% , CAS No.471-46-5

CAS: 471-46-5 Cat. No.: O113868 Peso molecular: 88.07 Beilstein Registry Number: 1743262 Número EC: 207-442-5

GRADE & PURITY ≥98%

Synonyms

ETHANEDIOIC ACID DIAMIDE | Formimidic acid, 1-carbamoyl- | WLN: ZVVZ | Oxamimidic acid | OXAMIDE | Amid kyseliny stavelove [Czech] | Oxamicacid amide | Amid kyseliny stavelove | D70377 | MFCD00008007 | FT-0632177 | NCI60_002253 | Oxalic acid diamide | AI3

Storage

Room temperature

Shipped In

Normal

Descripción general

Oxamide can be used:

· As a precursor for the synthesis of ligands such as bis(benzimidazole) and Schiff base ligands formed by condensation with furfural.

· Carbon nitride (g-C3N4) nanotubes by self-assembly polymerization with urea.

· As a bridging ligand for the synthesis of binuclear IrIII complex [Ir2(μ2-oxamidato-N,N′,O,O′)(ptpy)4], ptpy = 2-(p-tolyl)pyridinato

Specifications

Sinónimos

ETHANEDIOIC ACID DIAMIDE | Formimidic acid, 1-carbamoyl- | WLN: ZVVZ | Oxamimidic acid | OXAMIDE | Amid kyseliny stavelove [Czech] | Oxamicacid amide | Amid kyseliny stavelove | D70377 | MFCD00008007 | FT-0632177 | NCI60_002253 | Oxalic acid diamide | AI3

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488181082
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488181082
• Sonrisas canónicas: C(=O)(C(=O)N)N
• IUPAC Name: oxamide
• InChIKey: YIKSCQDJHCMVMK-UHFFFAOYSA-N
• INCHI: 1S/C2H4N2O2/c3-1(5)2(4)6/h(H2,3,5)(H2,4,6)
• Isómeros SMILES: C(=O)(C(=O)N)N
• WGK Alemania: 3
• RTECS: RO4900000
• Peso molecular: 88.07
• Beilstein: 1743262
• Reaxy-Rn: 1743262
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1743262&ln=

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Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in ethanol, slightly soluble in water and insoluble in diethyl ether.
• Punto de fusión (°C): 491°C
• Peso molecular: 88.070 g/mol
• XLogP3: -1.600
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 88.0273 Da
• Monoisotopic Mass: 88.0273 Da
• Topological Polar Surface Area: 86.200 Ų
• Heavy Atom Count: 6
• Formal Charge: 0
• Complexity: 75.500
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Jiayi Li, Ying Huang, Minhua Su, Yuying Xie, Diyun Chen.  (2021)  Dual light-driven p-ZnFe2O4/n-TiO2 catalyst: Benzene-breaking reaction for malachite green.  ENVIRONMENTAL RESEARCH,      [PMID:34597665] [10.1016/j.envres.2021.112081]

2. Guoqiang Zhang, Wei Huang, Yangsen Xu, Yongliang Li, Chuanxin He, Xiangzhong Ren, Peixin Zhang, Hongwei Mi.  (2023)  Suppressing Defects-Induced Non-Radiative Recombination for Activating the Near-Infrared Photoactivity of Red Polymeric Carbon Nitride.  ADVANCED FUNCTIONAL MATERIALS,  33  (52): (2305935).  [PMID:] [10.1002/adfm.202305935]

3. Ming Chen, Linyang Li, Lanlan Zhong, Chuanbao Xiao, Nianbing Zhong, Quanhua Xie, Dengjie Zhong, Yunlan Xu, Haixing Chang.  (2023)  Complete removal of 4-fluorophenol using a novel optical fiber photocatalysis–biodegradation–ion-adsorption system.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.142631]

4. Xue Bai, Jiangna Xing, Xin Huang, Shiyu Sun, Na Wang, Ting Wang, Hongxun Hao.  (2025)  3D spongy porous g-C3N4 material synthesized by supramolecular self-assembly for efficient degradation of tetracycline.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.162782]

5. Nanzhi Zheng, Yuchen Yang, Wenhao Huang, Jianting Zhang, Guohua Chen.  (2025)  Boric Acid-Catalyzed Synthesis: A scalable strategy for High-Yield and Tunable red fluorescent carbon dots.  SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY,      [PMID:40523329] [10.1016/j.saa.2025.126562]

6. Hao Zeng, Xiangbing Zou, Shuo Yang, Sizhe Tang, Shanshan Luo, Meiyue Cheng, Haiping Xu, Yujie Song, Ming Liu, Yang Liu, Ming Yang, Bing Li.  (2026)  Functional group engineering for boosting catalytic activity: high turnover frequency in electrocatalytic CO2 reduction and Zn-CO2 batteries.  JOURNAL OF COLLOID AND INTERFACE SCIENCE,      [PMID:41621356] [10.1016/j.jcis.2026.139983]