(+)-CUPARENE

Product Name: (+)-CUPARENE
CAS No.: 16982-00-6
Chemical Name: (+)-CUPARENE
Synonyms: (+)-CUPARENE;(R)-Cuparene;CUPARENE, (+);Einecs 241-061-5;(+) Cuparene,(+)Cuparene;(+)-Cuparene in isooctane;(+)-Cuparene, 10 mM in DMSO;(R)-1-(P-TOLYL)-1,2,2-TRIMETHYLCYCLOPENTANE;(R)-(+)-p-(1,2,2-trimethylcyclopentyl)toluene;(+)-Cuparene >=99.0% (sum of enantiomers, GC)
CBNumber: CB2176723
Molecular Formula: C15H22
Formula Weight: 202.34
MOL File: 16982-00-6.mol

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(+)-CUPARENE Property

Boiling point:: 275 °C(lit.)
Density: 0.937 g/mL at 20 °C(lit.)
refractive index: n20/D 1.523
Flash point:: 110℃
storage temp.: 2-8°C
optical activity: [α]20/D +64±2°, neat
BRN: 2326949
LogP: 6.210

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Safety

Hazard Codes: Xn
Risk Statements: 22
Safety Statements: 26-36
WGK Germany: 3
F: 10-23

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Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H302Harmful if swallowed

Precautionary statements

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

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

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N-Bromosuccinimide Price

Sigma-Aldrich

Product number: 28255
Product name: (+)-Cuparene
Purity: ≥99.0% (sum of enantiomers, GC)
Packaging: 1ml
Price: $604
Updated: 2025/07/31

American Custom Chemicals Corporation

Product number: HBL0000066
Product name: (+)-CUPARENE
Purity: 95.00%
Packaging: 1ML
Price: $982.33
Updated: 2021/12/16

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(+)-CUPARENE Chemical Properties,Usage,Production

Uses

Cuparene ((R)-Cuparene) is a sesquiterpenoid and can be isolated from Cupressaceae[1].

Definition

ChEBI: Cuparene is a sesquiterpenoid.

References

[1] Grantham P J, Douglas A G. The nature and origin of sesquiterpenoids in some Tertiary fossil resins[J]. Geochimica et Cosmochimica Acta, 1980, 44(11): 1801-1810.

(+)-CUPARENE Preparation Products And Raw materials

Raw materials

Preparation Products

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16982-00-6, (+)-CUPARENERelated Search:

(S)-(-)-Cuparene,(S)-Cuparene,(+)-CUPARENE,CUPARENE, (+) CUPARENE, (+)-(RG) 1-(1-ETHYL-PROPYL)-4-METHYL-BENZENE BENZENE, 1-CYCLOPENTYL-4-METHYL- NEOPENTYLBENZENE CYCLOPENTYLBENZENE (+)-CUPARENE

(+)-CUPARENE

CUPARENE, (+)

(R)-Cuparene

1-Methyl-4-(1,2,2-trimethylcyclopentyl)benzene

2,2-trimethylcyclopentyl)-1-methyl-4-((theta)-benzen

Benzene, 1-methyl-4-(1,2,2-trimethylcyclopentyl)-, (R)-

Toluene, p-(1,2,2-trimethylcyclopentyl)-, (R)-(+)-

(R)-1-(P-TOLYL)-1,2,2-TRIMETHYLCYCLOPENTANE

(R)-(+)-p-(1,2,2-trimethylcyclopentyl)toluene

1-Methyl-4-[(1R)-1,2,2-trimethylcyclopentyl]benzene

4-[(R)-1,2,2-Trimethylcyclopentane-1β-yl]toluene

Benzene, 1-methyl-4-(1,2,2-trimethylcyclopentyl)-, (theta)-

Einecs 241-061-5

(R)-1-Methyl-4-(1,2,2-triMethylcyclopentyl)benzene

(+)-Cuparene >=99.0% (sum of enantiomers, GC)

Benzene, 1-methyl-4-[(1R)-1,2,2-trimethylcyclopentyl]-

(+) Cuparene,(+)Cuparene

(+)-Cuparene in isooctane

(+)-Cuparene, 10 mM in DMSO

16982-00-6

Organic Building Blocks

Asymmetric Synthesis

Arenes

Chiral Building Blocks