268607
Formamidine hydrochloride
97%
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About This Item
Fórmula lineal:
HN=CHNH2 · HCl
Número de CAS:
Peso molecular:
80.52
Beilstein/REAXYS Number:
3906935
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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assay
97%
form
solid
mp
84-87 °C (lit.)
SMILES string
Cl[H].[H]C(N)=N
InChI
1S/CH4N2.ClH/c2-1-3;/h1H,(H3,2,3);1H
Inchi Key
NMVVJCLUYUWBSZ-UHFFFAOYSA-N
Application
Formamidine hydrochloride was used in the synthesis of imidazoleglycerol phosphate (IGP). It was also used in the synthesis of 5-methyl-4,6-dihydroxypyrimidine.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
Certificados de análisis (COA)
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The biosynthesis of histidine; D-erythro-imidazoleglycerol phosphate dehydrase.
B N AMES
The Journal of biological chemistry, 228(1), 131-143 (1957-09-01)
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A series of poly(fluorene-co-phenylene)-based anionic conjugated polyelectrolytes (CPEs) are prepared with varying sizes of counterions (tetramethylammonium, tetraethylammonium, and tetrabutylammonium (TBA+)) and studied as a hole-transporting layer (HTL) for sky-blue-emissive perovskite light-emitting diodes (PeLEDs). Ionic CPE HTLs improve the wettability, compatibility
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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
Shulin Chen et al.
Organic letters, 13(23), 6152-6155 (2011-11-02)
A new N-sulfonyl formamidine synthesis was developed via NaI-catalyzed direct condensation of sulfonamide and formamide. The green methodology is featured by high atom economy, easily available starting materials, the lack of need for a transition-metal catalyst, no requirement of hazardous
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