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(-)-TRANS-PINOCARVEOL

Product Name
(-)-TRANS-PINOCARVEOL
CAS No.
547-61-5
Chemical Name
(-)-TRANS-PINOCARVEOL
Synonyms
L-pinocarveol;(E)-Pinocarveol;laevo-pinocarveol;trans-Pinocarveole;L-trans-Pinocarveol;(-)-TRANS-PINOCARVEOL;Pinocarveol, trans-(-)-;(-)-TRANS-PINOCARVEOL 96+%;(1S,3R,5S)-2(10)-PINEN-3-OL;[1S,3R,5S,(-)]-Pin-2(10)-en-3-ol
CBNumber
CB9261778
Molecular Formula
C10H16O
Formula Weight
152.23
MOL File
547-61-5.mol
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(-)-TRANS-PINOCARVEOL Property

Melting point:
5 °C
Boiling point:
97-98 °C(Press: 12 Torr)
Density 
0.979 g/mL at 20 °C (lit.)
refractive index 
n20/D 1.500
form 
liquid
pka
14.91±0.40(Predicted)
color 
milky white
Odor
at 100.00 %. warm woody balsamic fennel
Odor Type
woody
optical activity
[α]20/D 72±3°, neat
BRN 
5730571
LogP
2.379 (est)
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Safety

Safety Statements 
23-24/25
WGK Germany 
3
F 
9-23
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Danger
Hazard statements

H315Causes skin irritation

H318Causes serious eye damage

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

P310Immediately call a POISON CENTER or doctor/physician.

P321Specific treatment (see … on this label).

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P362Take off contaminated clothing and wash before reuse.

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N-Bromosuccinimide Price

American Custom Chemicals Corporation
Product number
HBL0000013
Product name
(-)-TRANS-PINOCARVEOL
Purity
95.00%
Packaging
1ML
Price
$714.37
Updated
2021/12/16
AK Scientific
Product number
3412BA
Product name
(1S,5S)-6,6-Dimethyl-2-methylidenebicyclo[3.1.1]heptan-3-ol
Packaging
250mg
Price
$738
Updated
2021/12/16
AK Scientific
Product number
3412BA
Product name
(1S,5S)-6,6-Dimethyl-2-methylidenebicyclo[3.1.1]heptan-3-ol
Packaging
2.5g
Price
$2534
Updated
2021/12/16
AK Scientific
Product number
3412BA
Product name
(1S,5S)-6,6-Dimethyl-2-methylidenebicyclo[3.1.1]heptan-3-ol
Packaging
5g
Price
$3689
Updated
2021/12/16
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(-)-TRANS-PINOCARVEOL Chemical Properties,Usage,Production

Definition

ChEBI: (-)-trans-pinocarveol is the (1S,3R,5S)-stereoisomer of pinocarveol.

General Description

(-)-trans-Pinocarveol is an allyl alcohol. It is formed during the allylic oxidation of β-pinene using hydrogen peroxide-selenium dioxide or from the isomerization of α-pinene oxide over zirconium oxide.

(-)-TRANS-PINOCARVEOL Preparation Products And Raw materials

Raw materials

Preparation Products

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(-)-TRANS-PINOCARVEOL Suppliers

China 5 Germany 1 Switzerland 1 Ukraine 1 United States 6 Global 14
Service Chemical Inc.
Tel
--
Fax
--
Email
sales@chemos-group.com
Country
Germany
ProdList
6350
Advantage
71

547-61-5, (-)-TRANS-PINOCARVEOLRelated Search:

PINOCARVEOL (+)-BETA-PINENE (-)-TRANS-PINOCARVEOL

  • (1S,3R,5S)-6,6-DIMETHYL-2-METHYLENEBICYCLO[3.1.1]HEPTAN-3-OL
  • [1S-(1alpha,3alpha,5alpha)]-6,6-dimethyl-2-methylenebicyclo[3.1.1]heptan-3-ol
  • (-)-TRANS-PINOCARVEOL 96+%
  • (1S,3R,5S)-2-Methylene-6,6-dimethylbicyclo[3.1.1]heptane-3-ol
  • (1S,5S)-6,6-Dimethyl-2-methylenebicyclo[3.1.1]heptan-3α-ol
  • [1S,3R,5S,(-)]-Pin-2(10)-en-3-ol
  • (1S,5S)-6,6-dimethyl-2-methylene-norpinan-3-ol
  • (1S,5S)-7,7-dimethyl-4-methylidene-bicyclo[3.1.1]heptan-3-ol
  • (1S,5S)-7,7-dimethyl-4-methylidenebicyclo[3.1.1]heptan-3-ol
  • (-)-trans-Pinocarveol >=96.0% (sum of enantiomers, GC)
  • (E)-Pinocarveol
  • 2(10)-Pinen-3-ol, (1S,3R,5S)-(-)-
  • (1S,3R,5S)-2(10)-PINEN-3-OL
  • Bicyclo[3.1.1]heptan-3-ol, 6,6-dimethyl-2-methylene-, [1S-(1alpha,3alpha,5alpha)]-
  • L-pinocarveol
  • L-trans-Pinocarveol
  • Pinocarveol, trans-(-)-
  • trans-Pinocarveole
  • (-)-TRANS-PINOCARVEOL
  • Bicyclo[3.1.1]heptan-3-ol, 6,6-dimethyl-2-methylene-, (1S,3R,5S)-
  • laevo-pinocarveol
  • 1S-(1?,3?,5?)]-6,6-dimethyl-2-methylenebicyclo[3.1.1]heptan-3-ol
  • 547-61-5
  • Alcohols
  • Asymmetric Synthesis
  • Chiral Building Blocks
  • Organic Building Blocks