Skip to Content
Merck
CN

21335

(1R)-Camphor oxime

≥97.0% (sum of enantiomers, GC)

Synonym(s):

(1R)-1,7,7-Trimethylbicylco[2,2,1]heptan-2-one oxime

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Empirical Formula (Hill Notation):
C10H17NO
CAS Number:
Molecular Weight:
167.25
EC Number:
220-525-0
UNSPSC Code:
12352102
PubChem Substance ID:
Beilstein/REAXYS Number:
2413664
MDL number:
Assay:
≥97.0% (sum of enantiomers, GC)
Form:
solid
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI key

OVFDEGGJFJECAT-RZIOALPKSA-N

InChI

1S/C10H17NO/c1-9(2)7-4-5-10(9,3)8(6-7)11-12/h7,12H,4-6H2,1-3H3/b11-8+/t7-,10+/m1/s1

SMILES string

CC1(C)[C@@H]2CC[C@@]1(C)C(\C2)=N\O

assay

≥97.0% (sum of enantiomers, GC)

form

solid

optical activity

[α]20/D −40.5±1°, c = 5% in ethanol

mp

115-119 °C

functional group

oxime

Quality Level

Other Notes

Chiral intermediate; starting material for the preparation of R(+)-bornylamine and R(-)isobornylamine

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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

W. Huckel et al.
Justus Liebigs Annalen der Chemie, 625, 1-1 (1959)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service