Formamidine acetate - ≥99% , CAS No.3473-63-0

CAS: 3473-63-0 Cat. No.: F100557 Fórmula: CH₄N₂.C₂H₄O₂ Peso molecular: 104.11 Beilstein Registry Number: 3563488 Número CE: 222-442-5

GRADE & PURITY ≥99%

Synonyms

Formamidine acetate salt | Formamidinium acetate

Storage

Store at 2-8°C,Argon charged

Shipped In

Wet ice

Visão geral

Application

Formamidine acetate is used as an intermediate in the synthesis of active pharmaceutical ingredients. It is also used as a condensing agent for the preparation of pyrimidine and imidazole heterocycles. 

Specifications

Sinónimos

Formamidine acetate salt | Formamidinium acetate

Especificações e pureza

≥99%

Condições de armazenamento de armazenamento

Store at 2-8°C,Argon charged

Enviado em

Wet ice

Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.

Pureza

≥99%

Nomes e identificadores

Pubchem Sid

508811924

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/508811924

Sorrisos canónicos

CC(=O)O.C(=N)N

IUPAC Name

acetic acid;methanimidamide

InChIKey

XPOLVIIHTDKJRY-UHFFFAOYSA-N

INCHI

1S/C2H4O2.CH4N2/c1-2(3)4;2-1-3/h1H3,(H,3,4);1H,(H3,2,3)

SMILES isoméricas

CC(=O)O.C(=N)N

WGK Alemanha

2

Peso molecular

104.11

Beilstein

3563488

Reaxy-Rn

3563488

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3563488&ln=

Taxonomic Classification

Taxonomy Tree

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

• Kingdom: Organic compounds
• Superclass: Organic acids and derivatives
• Classe: Carboxylic acids and derivatives
• Subclass: Carboxylic acids
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxylic acids
• Alternative Parents: Monocarboxylic acids and derivatives Formamidines Carboximidamides Carboxamidines Organopnictogen compounds Organic oxides Imines Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Not available
• Substituents: Amidine - Formamidine - Carboxylic acid amidine - Carboxylic acid - Monocarboxylic acid or derivatives - Carboximidamide - Organic nitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organic oxide - Imine - Organopnictogen compound - Organic oxygen compound - Carbonyl group - Aliphatic acyclic compound
• Descrição: This compound belongs to the class of organic compounds known as carboxylic acids. These are compounds containing a carboxylic acid group with the formula -C(=O)OH.
• 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

Propriedades químicas e físicas

• Solubilidade: Soluble in water and hot alcohol.
• Sensibilidade: Hygroscopic.
• Ponto de fusão (°C): 162-164°C
• Peso molecular: 104.110 g/mol
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 0
• Exact Mass: 104.059 Da
• Monoisotopic Mass: 104.059 Da
• Topological Polar Surface Area: 87.200 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 41.300
• 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: 2

XLogP3