Idrazide formica - ≥90% , CAS No.624-84-0

CAS: 624-84-0 Cat. No.: F109757 Formula: CH₄N₂O Peso molecolare: 60.06 Beilstein Registry Number: 635759 Numero EC: 210-867-9

GRADE & PURITY ≥90%

Synonyms

Formoidrazide; Formilidrazide; Formilidrazina; Monoformilidrazina; N-Formilidrazina; NSC 72391 | F11944 | V1D8X13QFN | XZBIXDPGRMLSTC-UHFFFAOYSA- | Formidrazide | J-521389 | BCP26005 | 4-02-00-00085 (riferimento al manuale di Beilstein) | Idrazina formale

Storage

Conservare a 2-8°C, con carica di argon

Shipped In

Ghiaccio umido

Panoramica

L'idrazide formica è stata utilizzata nella sintesi di derivati dell'1,2,4-triazolo. È stata utilizzata anche nella sintesi di un nuovo agente antitumorale, il 6-N-formilamino-12,13-diidro-1,11-diidrossi-13-(β-D-glucopiranosil)-5H-indolo[2,3-a]-pirrolo[3,4-c]carbazolo-5,7(6H)-dione

Specifications

Sinonimi

Formoidrazide; Formilidrazide; Formilidrazina; Monoformilidrazina; N-Formilidrazina; NSC 72391 | F11944 | V1D8X13QFN | XZBIXDPGRMLSTC-UHFFFAOYSA- | Formidrazide | J-521389 | BCP26005 | 4-02-00-00085 (riferimento al manuale di Beilstein) | Idrazina formale

Specifiche e purezza

≥90%

Condizioni di conservazione di stoccaggio

Conservare a 2-8°C, con carica di argon

Spedito in

Ghiaccio umido

Purezza

≥90%

Nomi e identificatori

• Pubchem Sid: 508814961
• Sorrisi canonici: C(=O)NN
• IUPAC Name: formohydrazide
• InChIKey: XZBIXDPGRMLSTC-UHFFFAOYSA-N
• INCHI: 1S/CH4N2O/c2-3-1-4/h1H,2H2,(H,3,4)
• Isomeri SMILES: C(=O)NN
• WGK Germania: 3
• RTECS: LQ8615000
• Peso molecolare: 60.06
• Beilstein: 635759
• Reaxy-Rn: 635759
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=635759&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Classe Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxylic acid hydrazides
• Alternative Parents: Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Carboxylic acid hydrazide - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound
• Descrizione: This compound belongs to the class of organic compounds known as carboxylic acid hydrazides. These are carboxylic acid derivatives containing a carbonyl group in which the carbon is directly linked to a hydrazide group (N-N).
• External Descriptors: Not available

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Proprietà chimiche e fisiche

• Solubilità: Soluble in water, ethanol and acetone.
• Sensibilità: heat & Moisture sensitive
• Punto di infiammabilità (°F): 233.6 °F
• Punto di infiammabilità (°C): 112℃
• Punto di ebollizione (°C): 90 °C/0.7 mmHg
• Punto di fusione (°C): 52-57°C
• Peso molecolare: 60.056 g/mol
• XLogP3: -2.000
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 60.0324 Da
• Monoisotopic Mass: 60.0324 Da
• Topological Polar Surface Area: 55.100 Ų
• Heavy Atom Count: 4
• Formal Charge: 0
• Complexity: 20.000
• 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

Riferimenti

1. Jingyi Zhang, Zidan Cao, Di Fan, Yu Li, Tao Li, Baozeng Ren.  (2023)  Solid-liquid phase equilibrium of adiphenine hydrochloride in twelve pure solvents.  JOURNAL OF CHEMICAL THERMODYNAMICS,      [PMID:] [10.1016/j.jct.2023.107067]

2. Jianhang Qi, Jiale Liu, Yongming Ma, Yanjie Cheng, Kai Chen, Wenjing Hu, Junwei Xiang, Xiaoru Wang, Jianwei Zhao, Yang Zhou, Anyi Mei, Hongwei Han.  (2024)  Modulating Dual Functionalities of Hydrazide Derivatives for Iodide Oxidation Suppression and Defect Passivation in Printable Mesoscopic Perovskite Solar Cells.  Advanced Energy Materials,      [PMID:] [10.1002/aenm.202402344]

3. Pengshuai Zhang, Haiyan Luo, Lan Cui, Jixiu Deng, Shiyu Xie, Danfeng Liu, Shuqi Wang, Xiaoying Si, Zichao Wang, Yameng Wan, En Zhang, Xing Li, Lu Zhang.  (2022)  Assessment of solid–liquid equilibrium behavior and thermodynamic analysis of natural plant extracts artemisinin (Form I) in twelve mono-solvents.  JOURNAL OF MOLECULAR LIQUIDS,      [PMID:] [10.1016/j.molliq.2022.120975]