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340367

Sigma-Aldrich

(1R)-(−)-Nopol

98%

Synonym(s):

(−)-Nopol, (1R)-6,6-Dimethylbicyclo[3.1.1]hept-2-ene-2-ethanol, 6,6-Dimethyl-2-norpinene-2-ethanol, 6,6-Dimethylbicyclo[3.1.1]hept-2-ene-2-ethanol

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About This Item

Empirical Formula (Hill Notation):
C11H18O
CAS Number:
Molecular Weight:
166.26
Beilstein:
3196379
EC Number:
MDL number:
UNSPSC Code:
12352002
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

form

viscous liquid

optical activity

[α]24/D −37°, neat

refractive index

n20/D 1.493 (lit.)

bp

230-240 °C (lit.)

density

0.973 g/mL at 25 °C (lit.)

functional group

hydroxyl

SMILES string

CC1(C)[C@H]2CC=C(CCO)[C@@H]1C2

InChI

1S/C11H18O/c1-11(2)9-4-3-8(5-6-12)10(11)7-9/h3,9-10,12H,4-7H2,1-2H3/t9-,10-/m0/s1

InChI key

ROKSAUSPJGWCSM-UWVGGRQHSA-N

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General description

(1R)-(-)-Nopol is a chiral terpenol derivative.

Application

(1R)-(-)-Nopol may be used in the preparation of optically active O,O-diterpenyl dithiophosphoric and O-terpenyl aryldithiophosphonic acids by reacting with tetraphosphorus decasulfide and 2,4-diaryl 1,3,2,4-dithiadiphosphetane-2,4-disulfides, respectively. It may also react with silver hexafluoroantimonate to form a complex, which can be an effective initiator for the nonthermal curing of epoxy resins by electron beam induced cationic polymerization.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

208.4 °F - closed cup

Flash Point(C)

98 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Silver olefin complexes: highly efficient initiators for the electron beam curing of epoxy resins.
Barriau E, et al.
Macromolecules, 41(11), 3779-3781 (2008)
Terpene Analogues of Dithiophospate Pesticides.
Cherkasov RA, et al.
Phosph. Sulfur Relat. Elem., 186(4), 1003-1004 (2011)

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