CAS 622-33-3
:O-Benzylhydroxylamine
Description:
O-Benzylhydroxylamine is an organic compound characterized by the presence of a hydroxylamine functional group attached to a benzyl group. Its molecular structure features a hydroxylamine (-NH2OH) moiety, which is known for its ability to act as a nucleophile and participate in various chemical reactions, including the formation of oximes from carbonyl compounds. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. O-Benzylhydroxylamine is soluble in polar solvents such as water and alcohols, which enhances its utility in organic synthesis. It is often used in the preparation of oximes and as a reagent in organic chemistry for the detection and quantification of carbonyl compounds. Additionally, it exhibits potential applications in medicinal chemistry due to its ability to modify biological molecules. However, like many organic compounds, it should be handled with care, as it may pose health risks if ingested or inhaled. Proper safety protocols should be followed when working with this substance.
Formula:C7H9NO
InChI:InChI=1S/C7H9NO/c8-9-6-7-4-2-1-3-5-7/h1-5H,6,8H2
InChI key:InChIKey=XYEOALKITRFCJJ-UHFFFAOYSA-N
SMILES:C(ON)C1=CC=CC=C1
Synonyms:- Akos B022277
- Aurora Ka-2549
- Aurora Ka-7528
- Benzyloxyamine
- Benzyloxyamine Hcl
- Hydroxylamine, O-(phenylmethyl)-
- Hydroxylamine, O-Benzyl-
- Labotest-Bb Lt00233131
- O-(Phenylmethyl)hydroxylamine
- O-Benzyloxyamine
- Snr 1635
- α-(Aminooxy)toluene
- See more synonyms
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 6 products.
O-Benzylhydroxylamine
CAS:<p>O-Benzylhydroxylamine</p>Formula:C7H9NOPurity:97%Color and Shape: clear. almost colourless liquidMolecular weight:123.15g/molO-Benzylhydroxylamine
CAS:Controlled Product<p>Applications O-Benzylhydroxylamine (cas# 622-33-3) is a useful research chemical.<br></p>Formula:C7H9NOColor and Shape:NeatMolecular weight:123.15O-Benzylhydroxylamine
CAS:<p>O-Benzylhydroxylamine is an antimicrobial agent that has been shown to be active against a range of microorganisms, including bacteria, fungi, and protozoa. It also has been shown to have an effect on locomotor activity in mice. O-Benzylhydroxylamine is synthesized by the asymmetric addition of hydrogen bromide to hydroxylamine with the use of a chiral catalyst. The synthesis yields two diastereomers, one enantiomeric form being active and the other inactive. O-Benzylhydroxylamine has been found to decrease levels of dopamine β-hydroxylase in rats and was used for the treatment of diabetic neuropathy and inflammatory bowel disease in human clinical trials.</p>Formula:C7H9NOPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:123.15 g/molO-Benzylhydroxylamine, 96%
CAS:<p>O-benzylhydroxylamine used in the synthesis of alfa- hydroxybenzylamines from alfa-hydroxyketones. It is also involved in the preparation of hydroxylamines and hydroxyamates. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation a</p>Formula:C7H10ClNOPurity:96%Color and Shape:Liquid, Clear colorless to white to yellowMolecular weight:159.61





