FACl - ≥99.5%(4 Times Purification) , CAS No.6313-33-3

CAS: 6313-33-3 Cat. No.: F492012 Formule: CH₄N₂·HCl Poids moléculaire: 80.52 Beilstein Registry Number: 3906935 Numéro CE: 228-639-2

QUALITÉ & PURETÉ ≥99.5%(4 Times Purification)

Synonyms

FORMAMIDINE, HYDROCHLORIDE | FT-0626527 | SB75370 | AKOS000260178 | Formimidamide hydrochloride | 2-hydroxy-4-methyl-3-nitro pyridine | FORMAMIDINE, MONOHYDROCHLORIDE | F0103 | formamidine HCl salt | NMVVJCLUYUWBSZ-UHFFFAOYSA-N | MFCD00012865 | A15719 | A

Storage

Protected from light,Room temperature,Argon charged

Shipped In

Normal

Vue d’ensemble

Application：

5-Methyl-4,6-dihydroxypyrimidine was synthesized from formamidine hydrochloride. N-Formimino-n-glutamate was synthesized from formamidine hydrochloride. Formamidine hydrochloride was used in the synthesis of imidazoleglycerol phosphate (IGP).

Spécifications

Synonymes

FORMAMIDINE, HYDROCHLORIDE | FT-0626527 | SB75370 | AKOS000260178 | Formimidamide hydrochloride | 2-hydroxy-4-methyl-3-nitro pyridine | FORMAMIDINE, MONOHYDROCHLORIDE | F0103 | formamidine HCl salt | NMVVJCLUYUWBSZ-UHFFFAOYSA-N | MFCD00012865 | A15719 | A

Spécifications et pureté

≥99.5%(4 Times Purification)

Conditions de stockage de stockage

Protected from light,Room temperature,Argon charged

Expédié en

Normal

Pureté

≥99.5%(4 Times Purification)

Noms et identifiants

Pubchem Sid

504765387

Pubchem Sid Url

https://pubchem.ncbi.nlm.nih.gov/substance/504765387

Sourires canoniques

C(=N)N.Cl

IUPAC Name

methanimidamide;hydrochloride

InChIKey

NMVVJCLUYUWBSZ-UHFFFAOYSA-N

INCHI

1S/CH4N2.ClH/c2-1-3;/h1H,(H3,2,3);1H

Isomères SMILES

C(=N)N.Cl

WGK Allemagne

3

Poids moléculaire

80.52

Beilstein

3906935

Reaxy-Rn

3666426

Reaxys-RN_link_address

https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=3666426&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organic nitrogen compounds
    • Classe Organonitrogen compounds
      • Subclass Amidines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Classe: Organonitrogen compounds
• Subclass: Amidines
• Intermediate Tree Nodes: Not available
• Direct Parent: Carboxamidines
• Alternative Parents: Formamidines Carboximidamides Organopnictogen compounds Imines Hydrochlorides Hydrocarbon derivatives
• Molecular Framework: Aliphatic acyclic compounds
• Substituents: Formamidine - Carboximidamide - Carboxylic acid amidine - Organopnictogen compound - Hydrocarbon derivative - Hydrochloride - Imine - Aliphatic acyclic compound
• Description: This compound belongs to the class of organic compounds known as carboxamidines. These are carboxylic acid derivatives containing the amidine group.
• 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

Propriétés chimiques et physiques

• Solubilité: Soluble in EtOH, DMF, DMSO, water et al
• Sensibilité: Moisture sensitive；air sensitive；light sensitive
• Point de fusion (°C): 84-87°C
• Poids moléculaire: 80.520 g/mol
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 0
• Exact Mass: 80.0141 Da
• Monoisotopic Mass: 80.0141 Da
• Topological Polar Surface Area: 49.900 Ų
• Heavy Atom Count: 4
• Formal Charge: 0
• Complexity: 10.300
• 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