268607
甲脒 盐酸盐
97%
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线性分子式:
HN=CHNH2 · HCl
化学文摘社编号:
分子量:
80.52
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
228-639-2
Beilstein/REAXYS Number:
3906935
MDL number:
产品名称
甲脒 盐酸盐, 97%
InChI key
NMVVJCLUYUWBSZ-UHFFFAOYSA-N
InChI
1S/CH4N2.ClH/c2-1-3;/h1H,(H3,2,3);1H
SMILES string
Cl[H].[H]C(N)=N
assay
97%
form
solid
mp
84-87 °C (lit.)
functional group
amine
Quality Level
Application
盐酸甲脒用于合成磷酸咪唑甘油（IGP）。它也用于合成5-甲基-4,6-二羟基嘧啶。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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)
The biosynthesis of histidine; D-erythro-imidazoleglycerol phosphate dehydrase.
B N AMES
The Journal of biological chemistry, 228(1), 131-143 (1957-09-01)
Chung Hyeon Jang et al.
ACS nano, 14(10), 13246-13255 (2020-09-11)
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
Federico Bertasi et al.
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
Carsten Präsang et al.
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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