
CAS 622-33-3: O-Benzylhydroxylamine
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
- See more synonyms
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Found 7 products.
O-Benzylhydroxylamine
CAS:O-BenzylhydroxylamineFormula:C7H9NOPurity:97%Color and Shape: clear. almost colourless liquidMolecular weight:123.15g/molO-Benzylhydroxylamine, 96%
CAS: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 and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C7H10ClNOPurity:96%Color and Shape:Liquid, Clear colorless to white to yellowMolecular weight:159.61O-Benzylhydroxylamine, 97%
CAS:This Thermo Scientific Chemicals brand product was originally part of the Acros Organics product portfolio. Some documentation and label information may refer to the legacy brand. The original Acros Organics product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.Formula:C7H10ClNOPurity:97%Color and Shape:Clear colorless, LiquidMolecular weight:159.61O-Benzylhydroxylamine
CAS:Controlled ProductApplications O-Benzylhydroxylamine (cas# 622-33-3) is a useful research chemical.Formula:C7H9NOColor and Shape:NeatMolecular weight:123.15O-Benzylhydroxylamine
CAS: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.Formula:C7H9NOPurity:Min. 95%Color and Shape:Clear LiquidMolecular weight:123.15 g/mol