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Formamidin -hydrochlorid
97%
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About This Item
Empfohlene Produkte
Qualitätsniveau
Assay
97%
Form
solid
mp (Schmelzpunkt)
84-87 °C (lit.)
Funktionelle Gruppe
amine
SMILES String
Cl[H].[H]C(N)=N
InChI
1S/CH4N2.ClH/c2-1-3;/h1H,(H3,2,3);1H
InChIKey
NMVVJCLUYUWBSZ-UHFFFAOYSA-N
Anwendung
Formamidine hydrochloride was used in the synthesis of imidazoleglycerol phosphate (IGP). It was also used in the synthesis of 5-methyl-4,6-dihydroxypyrimidine.
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
Eyeshields, Gloves, type N95 (US)
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The biosynthesis of histidine; D-erythro-imidazoleglycerol phosphate dehydrase.
The Journal of biological chemistry, 228(1), 131-143 (1957-09-01)
Reactions of oxidizing radicals with 4, 6-dihydroxypyrimidines as model compounds for uracil, thymine, and cytosine.
The Journal of Physical Chemistry, 91(2), 426-433 (1987)
Physical chemistry chemical physics : PCCP, 19(38), 26230-26239 (2017-09-22)
This work describes the preparation of the new lipophilic ionic liquid tetraoctyl-formamidinium bis(trifluoromethanesulfonyl) imide (TOFATFSI), which is miscible with lower alkanes. In particular, this work focuses on the electric behaviour of TOFATFSI in the particularly challenging highly apolar environment of
Inorganic chemistry, 44(25), 9444-9452 (2005-12-06)
The preparation of the [NBu4][Pt(C6F5)3L] complexes (L=triazene, formamidine, 2-aminopyridine,) have been carried out. These ligands contain a hydrogen atom, with more or less acidic character, in a position suitable for establishing an intramolecular hydrogen bonding interaction with the metal center.
Journal of the American Chemical Society, 127(29), 10182-10183 (2005-07-21)
Carbene analogues of borazines are highly thermally stable. Keeping quasi-identical steric demands, the electronic properties of the carbene can be precisely tuned by varying the nature of the substituents at the boron centers.
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