47700
Formamidine hydrochloride
purum, ≥98.0% (AT)
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About This Item
Linear Formula:
HN=CHNH2 · HCl
CAS Number:
Molecular Weight:
80.52
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
228-639-2
MDL number:
Beilstein/REAXYS Number:
3906935
grade
purum
assay
≥98.0% (AT)
mp
79-85 °C
SMILES string
Cl.NC=N
Storage Class
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2
Regulatory Information
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Weiwen Zhao et al.
Organic letters, 13(19), 5160-5163 (2011-08-30)
N,N'-Disubstituted formamidines, and amidines in general, have very rich configurational, conformational, and tautomeric diversities. As part of an effort to incorporate alkoxyamine-derived formamidine units into foldamers, the first evidence for the isolation of the up-to-now unknown E isomer, the conditions
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
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.
José M Casas et al.
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.
Shridhar Bhat et al.
Bioorganic & medicinal chemistry, 20(14), 4507-4513 (2012-06-19)
Our previous target validation studies established that inhibition of methionine aminopeptidases (MtMetAP, type 1a and 1c) from Mycobacterium tuberculosis (Mtb) is an effective approach to suppress Mtb growth in culture. A novel class of MtMetAP1c inhibitors comprising of N'-hydroxy-N-(4H,5H-naphtho[1,2-d]thiazol-2-yl)methanimidamide (4c)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| U-003-1ML | 04061837820977 |
| D-167-1ML | 04061837817489 |
| D-168-1ML | 04061837817496 |
| I-045-1ML | 04061841811282 |
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