What is the (1S)-(1)-beta-Pinene?

(1S)-(1)-beta-Pinene is clear colorless to pale yellow liquid, while it's Molecular Formula is C10H16. clear colorless to pale yellow liquid (-)-ß-Pinene has been used as a standard for the analysis of terpenoid compounds in plant essential oils by GC analysis. It may be used as a building block to synthesize natural products such as grandisol, robustadial and (+)-nopinone. (-)-ß-Pinene undergoes hydroformylation in the presence of platinum/tin catalysts to form trans-10-formylpinane.

What is the CAS number for (1S)-(1)-beta-Pinene?

The CAS number of (1S)-(1)-beta-Pinene is 18172-67-3.

What is (1S)-(1)-beta-Pinene (18172-67-3) used for?

(–)-ß-Pinene is a bicyclic monoterpene that has been found in various plants, including C. sativa, with diverse biological activities. It is lethal to S. littoralis third instar larvae (LD50 = 65 µg/larva). (–)-ß-Pinene inhibits infectious bronchitis virus (IBV) replication (IC50 = 1.32 mM) and exhibits a cytotoxic concentration (CC50) value of greater than 10 mM in Vero cells. In vivo, (–)-ß-pinene (100 mg/kg) decreases immobility time in the forced swim test in mice, an effect that can be reversed by the serotonin (5-HT) receptor subtype 5-HT1A antagonist WAY-100635 .InChI:InChI=1/C10H16/c1-7-4-5-8-6-9(7)10(8,2)3/h8-9H,1,4-6H2,2-3H3/t8?,9-/m0/s1

What is the (1S)-(1)-beta-Pinene?

(1S)-(1)-beta-Pinene is clear colorless to pale yellow liquid, while it's Molecular Formula is C10H16. clear colorless to pale yellow liquid (-)-β-Pinene has been used as a standard for the analysis of terpenoid compounds in plant essential oils by GC analysis. It may be used as a building block to synthesize natural products such as grandisol, robustadial and (+)-nopinone. (-)-β-Pinene undergoes hydroformylation in the presence of platinum/tin catalysts to form trans-10-formylpinane.

What is the CAS number for (1S)-(1)-beta-Pinene?

The CAS number of (1S)-(1)-beta-Pinene is 18172-67-3.

What is (1S)-(1)-beta-Pinene (18172-67-3) used for?

(–)-β-Pinene is a bicyclic monoterpene that has been found in various plants, including C. sativa, with diverse biological activities. It is lethal to S. littoralis third instar larvae (LD50 = 65 μg/larva). (–)-β-Pinene inhibits infectious bronchitis virus (IBV) replication (IC50 = 1.32 mM) and exhibits a cytotoxic concentration (CC50) value of greater than 10 mM in Vero cells. In vivo, (–)-β-pinene (100 mg/kg) decreases immobility time in the forced swim test in mice, an effect that can be reversed by the serotonin (5-HT) receptor subtype 5-HT1A antagonist WAY-100635 .InChI:InChI=1/C10H16/c1-7-4-5-8-6-9(7)10(8,2)3/h8-9H,1,4-6H2,2-3H3/t8?,9-/m0/s1

Factory supply (1S)-(1)-beta-Pinene 18172-67-3 with sufficient production capacity

(1S)-(1)-beta-Pinene

CAS No.: 18172-67-3
Purity: 99%

Factory supply (1S)-(1)-beta-Pinene 18172-67-3 with sufficient production capacity

Molecular Formula: C10H16
Molecular Weight: 136.237
Appearance/Colour: clear colorless to pale yellow liquid
Vapor Pressure: ~2 mm Hg ( 20 °C)
Melting Point: -61 °C(lit.)
Refractive Index: n20/D 1.478
Boiling Point: 166 °C at 760 mmHg
Flash Point: 34.9 °C
PSA： 0.00000
Density: 0.88 g/cm³
LogP: 2.99870

(1S)-(1)-beta-Pinene(Cas 18172-67-3) Usage

InChI:InChI=1/C10H16/c1-7-4-5-8-6-9(7)10(8,2)3/h8-9H,1,4-6H2,2-3H3/t8?,9-/m0/s1

18172-67-3 Relevant articles

Isotopically Sensitive Branching as a Tool for Evaluating Multiple Product Formation by Monoterpene Cyclases

Wagschal, Kurt,Savage, Thomas J.,Croteau, Rodney

, p. 5933 - 5944 (1991)

The deuterated substrates geranyl pyroph...

Temperature Controls Guest Uptake and Release from Zn4L4 Tetrahedra

Zhang, Dawei,Ronson, Tanya K.,Güryel, Songül,Thoburn, John D.,Wales, David J.,Nitschke, Jonathan R.

, p. 14534 - 14538 (2019)

We report the preparation of triazatruxe...

Acorenone B: AChE and BChE inhibitor as a major compound of the essential oil distilled from the ecuadorian species niphogeton dissecta (Benth.) J.F. macbr

Calva, James,Bec, Nicole,Gilardoni, Gianluca,Larroque, Christian,Cartuche, Luis,Bicchi, Carlo,Montesinos, José Vinicio

, (2017/11/16)

This study investigated the chemical com...

Oxidation of cyclohexene and α-pinene with O2-H 2 mixture in the presence of supported platinum or palladium catalysts

Kuznetsova,Kuznetsova,Kirillova,Pokrovskii,Detusheva,Ancel,Likholobov

, p. 1544 - 1551 (2007/10/03)

Oxidation of cyclohexene and α-pinene wi...

The first regio- and diastereoselective synthesis of homochiral perhydroimidazoisoxazoles via the 1,3-dipolar cycloaddition of imidazoline 3-oxides with (1S)-(-)-β-pinene

Coskun, Necdet,Tat, Fatma Tirli,Gueven, Oezden Oezel

, p. 1463 - 1467 (2007/10/03)

The 1,3-dipolar cycloaddition of imidazo...

18172-67-3 Process route

: 7785-26-4,25766-18-1
(-)-α-pinene

: 18172-67-3,19902-08-0,25719-60-2
beta-pinene

Conditions

Conditions	Yield
With selenium(IV) oxide; ethanol;

: 380414-97-1
(1'R,2'S,5'S)-2-(2'-Hydroxy-6',6'-dimethylbicyclo[3.1.1]hept-2'-yl)acetic acid

: 18172-67-3,19902-08-0,25719-60-2
beta-pinene

Conditions

Conditions	Yield
With quinoline; at 200 ℃;

18172-67-3 Upstream products

7785-26-4
(-)-α-pinene
380414-97-1
(1'R,2'S,5'S)-2-(2'-Hydroxy-6',6'-dimethylbicyclo[3.1.1]hept-2'-yl)acetic acid
35836-73-8
(1R)-(-)-nopol
763-10-0
geranyl diphosphate