Skip to Content
Merck
CN

365181

N-Benzylhydroxylamine hydrochloride

97%

Sign In to View Organizational & Contract Pricing.

Select a Size

Change View

About This Item

Linear Formula:
C6H5CH2NHOH · HCl
CAS Number:
Molecular Weight:
159.61
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
507948
Assay:
97%
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist


assay

97%

mp

108-110 °C (lit.)

functional group

amine, phenyl

SMILES string

Cl.ONCc1ccccc1

InChI

1S/C7H9NO.ClH/c9-8-6-7-4-2-1-3-5-7;/h1-5,8-9H,6H2;1H

InChI key

YSNXOQGDHGUKCZ-UHFFFAOYSA-N

General description

N-Benzylhydroxylamine hydrochloride is a N-substituted-hydroxylamine. It participates in the ring opening of (2S,3R)-1,2-epoxy-4-penten-3-ol. Two-step synthesis of N-benzylhydroxylamine starting from dibenzylamine is reported.

Application

N-Benzylhydroxylamine hydrochloride may be used in the preparation of a precursor to hitherto unknown aminocyclopentitol derivative, hydroxy functionalised 4-exo-ethoxycarbonyl-3-oxa-2-azabicyclo[3.3.0]octane system.

Analysis Note

May contain traces of methyl orange, which can cause the color to take on a faint red hue.


Still not finding the right product?


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

新产品

This item has



Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library



[1, 3]-Dipolar intramolecular nitrone olefin cycloaddition reaction of a sugar-derived a, ?-unsaturated ester: a new diastereo-and regioselective synthesis of an aminocyclopentitol.
Jachak SM, et al.
Tetrahedron Letters, 42(29), 4925-4928 (2001)
The Synthesis of Chiral Polyhydroxylated Pyrrolidines Using a Reverse-Cope Cyclisation.
O'Neil IA, et al.
Synlett, 10, 1408-1410 (2000)
A Large-Scale Low-Cost Preparation of N-Benzylhydroxylamine Hydrochloride.
Nguyen TB, et al.
Synthesis, 18, 3174-3176 (2009)



Global Trade Item Number

SKUGTIN
365181-1G04061831825725