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Merck
CN

80585

蒎烷

purum, mixture of isomers, ≥98.0% (GC)

别名:

2,6,6-三甲基二环[3.1.1]庚烷

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关于此项目

经验公式(希尔记法):
C10H18
化学文摘社编号:
分子量:
138.25
EC Number:
207-467-1
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
5237941
MDL number:
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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



pictograms

FlameEnvironment

signalword

Warning

hcodes

Hazard Classifications

Aquatic Chronic 2 - Flam. Liq. 3

存储类别

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

法规信息

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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
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