Acetohydrazide - ≥98% , CAS No.1068-57-1

CAS: 1068-57-1 Cat. No.: A151537 Peso molecular: 74.08 Número EC: 213-948-7

GRADE & PURITY ≥98%

Synonyms

Hydrazid kyseliny octove | Acethydrazide (moist with methylene chloride) | BP-30010 | Hydrazine, acetyl- | Ald3.1-H_000952 | Hydrazid kyseliny octove [Czech] | AM20080014 | Ald3.1-H_000633 | CCRIS 4791 | OFLXLNCGODUUOT-UHFFFAOYSA- | Q4678005 | acetohydraz

Storage

Protected from light,Room temperature,Argon charged

Shipped In

Normal

Descripción general

Acethydrazide can be used in the synthesis of (E)-N′-(2-hydroxybenzylidene)acetohydrazide, an ONO pincer ligand.

Specifications

Sinónimos

Hydrazid kyseliny octove | Acethydrazide (moist with methylene chloride) | BP-30010 | Hydrazine, acetyl- | Ald3.1-H_000952 | Hydrazid kyseliny octove [Czech] | AM20080014 | Ald3.1-H_000633 | CCRIS 4791 | OFLXLNCGODUUOT-UHFFFAOYSA- | Q4678005 | acetohydraz

Especificaciones y pureza

≥98%

Condiciones de almacenamiento de almacenamiento

Protected from light, Room temperature, Argon charged

Enviado en

Normal

Pureza

≥98%

Nombres e identificadores

• Pubchem Sid: 488181925
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/488181925
• Sonrisas canónicas: CC(=O)NN
• IUPAC Name: acetohydrazide
• InChIKey: OFLXLNCGODUUOT-UHFFFAOYSA-N
• INCHI: 1S/C2H6N2O/c1-2(5)4-3/h3H2,1H3,(H,4,5)
• Isómeros SMILES: CC(=O)NN
• RTECS: AI1225000
• Peso molecular: 74.08
• Reaxy-Rn: 506165
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=506165&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic acids and derivatives
    • Clase Carboxylic acids and derivatives
      • Subclass Carboxylic acid derivatives
        • Level5 Carboxylic acid amides
          • Level6 Acetamides

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Clase: Carboxylic acids and derivatives
• Subclass: Carboxylic acid derivatives
• Intermediate Tree Nodes: Carboxylic acid amides
• Direct Parent: Acetamides
• Alternative Parents: Carboxylic acid hydrazides Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Acetamide - Carboxylic acid hydrazide - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic acyclic compound
• Descripción: This compound belongs to the class of organic compounds known as acetamides. These are organic compounds with the general formula RNHC(=O)CH3, where R= organyl group.
• External Descriptors: carbohydrazonic acid

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

Objetivos asociados (no humanos)

Escherichia coli (133304 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in water.DMSO (Slightly), Methanol (Slightly)
• Sensibilidad: Air & heat Sensitive,hygroscopic
• Punto de inflamación (°F): 235.4 °F
• Punto de inflamación (°C): 113 °C
• Punto de ebullición (°C): 134°C/21mmHg
• Punto de fusión (°C): 57-60°C
• Peso molecular: 74.080 g/mol
• XLogP3: -1.600
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 74.048 Da
• Monoisotopic Mass: 74.048 Da
• Topological Polar Surface Area: 55.100 Ų
• Heavy Atom Count: 5
• Formal Charge: 0
• Complexity: 42.900
• 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. Yang Li, Ling Ling, Chuan-Fan Ding.  (2023)  Isomer-specific quantification of human milk oligosaccharides based on Girard reagent P-d0/d5 derivatization and trapped ion mobility spectrometry-mass spectrometry.  JOURNAL OF FOOD COMPOSITION AND ANALYSIS,      [PMID:] [10.1016/j.jfca.2023.105874]

2. Yunsheng Xu, Chonglin Liu, Yanying Zhao, Xianming Zhang, Minna Hakkarainen.  (2024)  Photocurable acylhydrazone covalent adaptable networks with fast dynamic exchange and tunable viscoelastic properties.  Polymer Chemistry,  15  (22): (2253-2264).  [PMID:] [10.1039/D4PY00230J]

3. Jinbo Ouyang, Longping Jiang, Jiayao Li, Feiqiang He, Zhi Gao, Mengmeng Wang, Limin Zhou, Zongbo Xie, Zhiqiang Zhu, Yifu Chen.  (2025)  Light-Driven Crystal Actuation of Fluorinated Acylhydrazones Enabled by [2+2] Photocycloaddition.  CHEMISTRY-A EUROPEAN JOURNAL,      [PMID:40626992] [10.1002/chem.202501777]

4. Youbing Li, Chonglin Liu, Yunsheng Xu, Shuangfei Xiang, Wenjun Peng, Xianming Zhang, Minna Hakkarainen, Pengwu Xu, Weijun Yang, Piming Ma.  (2026)  Tuning Acylhydrazone Exchange Dynamics via Substituent Effects for Reprocessable and High-Resolution 3D Printable CANs.  ACS Applied Polymer Materials,      [PMID:] [10.1021/acsapm.5c03980]