B22984
O-Benzylhydroxylamine hydrochloride
99%
Synonym(s):
Benzyloxyamine hydrochloride
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All Photos(2)
About This Item
Linear Formula:
C6H5CH2ONH2 · HCl
CAS Number:
Molecular Weight:
159.61
Beilstein:
3687991
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
99%
form
crystals
mp
238 °C (subl.) (lit.)
SMILES string
Cl.NOCc1ccccc1
InChI
1S/C7H9NO.ClH/c8-9-6-7-4-2-1-3-5-7;/h1-5H,6,8H2;1H
InChI key
HYDZPXNVHXJHBG-UHFFFAOYSA-N
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Application
Effective reagent used to prepare α-hydroxybenzylamines from α-hydroxyketones.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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G Stampf et al.
Die Pharmazie, 35(1), 43-44 (1980-01-01)
The study of the blood levels and tissue concentrations in mice to which 14C-benzyloxyamine hydrochloride was applied in the form of a spray and of a suspensoid aerosol evidenced the good abosrption of this pharmacon. Maximum blood levels were observed
Tetrahedron Letters, 32, 711-711 (1991)
Yin Luo et al.
ChemMedChem, 7(9), 1587-1593 (2012-07-20)
Forty-three oxime derivatives were synthesized by allowing O-benzylhydroxylamines to react with primary benzaldehydes or salicylaldehydes; these products were gauged as potential inhibitors of β-ketoacyl-(acyl-carrier-protein) synthase III (FabH). Among the 43 compounds, 38 are reported herein for the first time. These
[Thermographic analysis of precipitates formed by the interaction of active ingredients and additives].
G Stampf et al.
Acta pharmaceutica Hungarica, 53(6), 268-272 (1983-11-01)
Samia Far et al.
Journal of peptide science : an official publication of the European Peptide Society, 11(7), 424-430 (2005-01-11)
The synthesis of glyoxylyl peptides by coupling the masked glyoxylic acid derivative (FmocNH)(2)CHCO(2)H, 1, to a peptidyl resin assembled using Fmoc/tert-butyl chemistry has been described recently. Deprotection and cleavage of the peptide from the solid support using TFA was followed
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