Alle Fotos(1)
Wichtige Dokumente
396788
Ethylformimidat -hydrochlorid
Synonym(e):
Ethyl methanimidate hydrochloride
Anmeldenzur Ansicht organisationsspezifischer und vertraglich vereinbarter Preise
Alle Fotos(1)
About This Item
Lineare Formel:
HC(=NH)OC2H5·HCl
CAS-Nummer:
Molekulargewicht:
109.55
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
Empfohlene Produkte
Form
solid
Qualitätsniveau
mp (Schmelzpunkt)
75 °C (dec.) (lit.)
Funktionelle Gruppe
ether
Lagertemp.
2-8°C
SMILES String
Cl.CCOC=N
InChI
1S/C3H7NO.ClH/c1-2-5-3-4;/h3-4H,2H2,1H3;1H
InChIKey
JPUTTYRVDANTBN-UHFFFAOYSA-N
Allgemeine Beschreibung
Ethyl formimidate hydrochloride is a nitrogen containing organic building block. On heating it undergoes degradation to afford formamidine hydrochloride, ethyl formate and ethyl chloride.
Anwendung
Ethyl formimidate hydrochloride may be used in the preparation of the following:
- 5-aminoimidazole-4-carboxylic acid α- and β-ribotides
- s-triazines
- 2,3:5,6-di-O-isopropylidene-α- and -β-5-amino-4-ethoxycarbonyl or -carbamoyl-imidazole D-mannofuranosides
- 5-amino-1-(2-pyridyl)imidazole
Reactant involved in the synthesis of biologically active molecules including:
Reactant involved in:
- Bredinin via amination of an acyclic precursor
- Amidine conjugates of the ornithine moiety of an antifungal
Reactant involved in:
- Intermolecular cyclization
- Mo-catalyzed asymmetric ring-closing metathesis for synthesis of cyclid amides and amines
- Synthesis of peptidic 1-cyanopyrrolidines
Signalwort
Warning
H-Sätze
Gefahreneinstufungen
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Zielorgane
Respiratory system
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
dust mask type N95 (US), Eyeshields, Gloves
Hier finden Sie alle aktuellen Versionen:
Besitzen Sie dieses Produkt bereits?
In der Dokumentenbibliothek finden Sie die Dokumentation zu den Produkten, die Sie kürzlich erworben haben.
Purines, pyrimidines, and imidazoles part 54. Interconversion of some intermediates in the de novo biosynthesis of purine nucleotides.
Cusack NJ, et al.
Journal of the Chemical Society. Perkin Transactions 1, 2316-2321 (1980)
Purines, pyrimidines, and imidazoles. Part XLI. Glycofuranosylamines derived from D-xylose, D-glucose, D-mannose, and L-rhamnose and their use in the synthesis of pyrimidine and imidazole nucleosides.
Cusack NJ, et al.
Journal of the Chemical Society. Perkin Transactions 1, 73-81 (1974)
Purines, pyrimidines, and imidazoles. XL. A new synthesis of a D-ribofuranosylamine derivative and its use in the synthesis of pyrimidine and imidazole nucleosides.
N J Cusack et al.
Journal of the Chemical Society. Perkin transactions 1, 16, 1720-1731 (1973-01-01)
Synthesis of the S-Triazine System. Iii. 1 Trimerization of Imidates.
Schaefer FC and Peters GA.
The Journal of Organic Chemistry, 26(8), 2771-2784 (1961)
Rhodd EH and von Richter V.
Chemistry of Organic Compounds: Pt. B. Aliphatic compounds, 551-551 (1951)
Unser Team von Wissenschaftlern verfügt über Erfahrung in allen Forschungsbereichen einschließlich Life Science, Materialwissenschaften, chemischer Synthese, Chromatographie, Analytik und vielen mehr..
Setzen Sie sich mit dem technischen Dienst in Verbindung.