80585
Pinane
purum, mixture of isomers, ≥98.0% (GC)
Synonym(s):
2,6,6-Trimethylbicyclo[3.1.1]heptane
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About This Item
Empirical Formula (Hill Notation):
C10H18
CAS Number:
Molecular Weight:
138.25
EC Number:
207-467-1
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
5237941
MDL number:
grade
purum
assay
≥98.0% (GC)
density
0.857 g/mL at 20 °C (lit.)
SMILES string
CC1CC[C@@H]2C[C@H]1C2(C)C
InChI
1S/C10H18/c1-7-4-5-8-6-9(7)10(8,2)3/h7-9H,4-6H2,1-3H3/t7?,8-,9-/m1/s1
InChI key
XOKSLPVRUOBDEW-CFCGPWAMSA-N
signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 2 - Flam. Liq. 3
Storage Class
3 - Flammable liquids
wgk
WGK 3
flash_point_f
107.6 °F
flash_point_c
42 °C
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
Regulatory Information
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Valérie Capra et al.
PloS one, 8(3), e60475-e60475 (2013-04-05)
The intrahelical salt bridge between E/D(3.49) and R(3.50) within the E/DRY motif on helix 3 (H3) and the interhelical hydrogen bonding between the E/DRY and residues on H6 are thought to be critical in stabilizing the class A G protein-coupled
Achim Stolle et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 14(22), 6805-6814 (2008-06-20)
Catalyzed and uncatalyzed rearrangement reactions of terpenoids play a major role in laboratory and industrial-scale synthesis of fine chemicals. Herein, we present our results on the thermally induced isomerization of pinane (1). Investigation of the thermal behavior of (+)-cis- (1
Yue Song et al.
Journal of separation science, 31(1), 64-70 (2007-12-21)
In this study, a rapid and reliable assay has been developed for quantification of pinane monoterpene glycosides in cortex Moutan; it is based on capillary high performance liquid chromatography coupled with electrospray ionization mass spectrometry (capillary HPLC-ESI MS). This method
A von Matt et al.
Bioorganic & medicinal chemistry, 8(9), 2291-2303 (2000-10-12)
Based on the structural comparison of the S1 pocket in different trypsin-like serine proteases, a series of Boc-D-trimethylsilylalanine-proline-boro-X pinanediol derivatives, with boro-X being different amino boronic acids, have been synthesized as inhibitors of thrombin. Among the novel compounds, a number
Zsolt Szakonyi et al.
Amino acids, 41(3), 597-608 (2011-03-31)
Natural monoterpenes have proved to be good starting materials for the synthesis of β-amino acid derivatives. In the past decade, a number of well-known synthetic procedures have been applied for the preparation of monoterpene-based β-amino acid derivatives, e.g. from β-lactams
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