O-Benzylhydroxylamine hydrochloride - CAS 2687-43-6
Catalog: |
BB019387 |
Product Name: |
O-Benzylhydroxylamine hydrochloride |
CAS: |
2687-43-6 |
Synonyms: |
O-benzylhydroxylamine;hydrochloride |
IUPAC Name: | O-benzylhydroxylamine;hydrochloride |
Description: | A reagent used for the synthesis of hydroxylamines and hydroxyamates. |
Molecular Weight: | 159.61 |
Molecular Formula: | C7H10ClNO |
Canonical SMILES: | C1=CC=C(C=C1)CON.Cl |
InChI: | InChI=1S/C7H9NO.ClH/c8-9-6-7-4-2-1-3-5-7;/h1-5H,6,8H2;1H |
InChI Key: | HYDZPXNVHXJHBG-UHFFFAOYSA-N |
Boiling Point: | 237.5 °C at 760 mmHg |
Purity: | 97 % |
Appearance: | White to light yellow crystal powde |
MDL: | MFCD00012952 |
LogP: | 2.57920 |
GHS Hazard Statement: | H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation] |
Precautionary Statement: | P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Warning |
Publication Number | Title | Priority Date |
CN-112656791-A | Compound for treating maple syrup urine disease | 20210201 |
CN-112645835-A | Preparation method of benzyloxyamine hydrochloride | 20201219 |
JP-2021006531-A | Cross-linked conjugate for conjugation of cell-binding molecules | 20200901 |
CN-111909292-A | Preparation method and application of O-benzylhydroxylamine resin | 20200814 |
CN-111848463-A | Camphor sulfanilamide oxime ether compound and preparation method and application thereof | 20200708 |
PMID | Publication Date | Title | Journal |
22811397 | 20120901 | Synthesis and antimicrobial activities of oximes derived from O-benzylhydroxylamine as FabH inhibitors | ChemMedChem |
19032949 | 20090109 | Acrolein toxicity: Comparison with reactive oxygen species | Biochemical and biophysical research communications |
17889592 | 20080601 | Synthesis and NMR spectral studies of some 2,6-diarylpiperidin-4-one O-benzyloximes | Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy |
17688325 | 20070901 | Regiospecific solid-phase strategy to N7-substituted purines and its application to 8-azapurines and [I]-condensed purines | Journal of combinatorial chemistry |
15641117 | 20050701 | Synthesis of glyoxylyl peptides using an Fmoc-protected alpha,alpha'-diaminoacetic acid derivative | Journal of peptide science : an official publication of the European Peptide Society |
Complexity: | 69.3 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 2 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 159.0450916 |
Formal Charge: | 0 |
Heavy Atom Count: | 10 |
Hydrogen Bond Acceptor Count: | 2 |
Hydrogen Bond Donor Count: | 2 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 159.0450916 |
Rotatable Bond Count: | 2 |
Topological Polar Surface Area: | 35.2 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
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