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

CAS: 6313-33-3 Cat. No.: F492012 Summenformel: CH₄N₂·HCl Molekulargewicht: 80.52 Beilstein Registry Number: 3906935 EG-Nummer: 228-639-2

QUALITÄT & REINHEIT ≥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

Übersicht

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).

Spezifikationen

Synonyme

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

Spezifikationen & Reinheit

≥99.5%(4 Times Purification)

Storage

Protected from light,Room temperature,Argon charged

Verschickt in

Normal

Reinheit

≥99.5%(4 Times Purification)

Namen und Kennungen

Pubchem Sid

504765387

Pubchem Sid Url

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

Kanonisches Lächeln

C(=N)N.Cl

IUPAC Name

methanimidamide;hydrochloride

InChIKey

NMVVJCLUYUWBSZ-UHFFFAOYSA-N

INCHI

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

Isomere SMILES

C(=N)N.Cl

WGK Deutschland

3

Molekulargewicht

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
    • Klasse Organonitrogen compounds
      • Subclass Amidines

• Kingdom: Organic compounds
• Superclass: Organic nitrogen compounds
• Klasse: 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
• Beschreibung: 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

Chemische und physikalische Eigenschaften

• Löslichkeit: Soluble in EtOH, DMF, DMSO, water et al
• Empfindlichkeit: Moisture sensitive；air sensitive；light sensitive
• Schmelzpunkt (°C): 84-87°C
• Molekulargewicht: 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