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28255

Sigma-Aldrich

(+)-Cuparene

≥99.0% (sum of enantiomers, GC)

Synonym(s):

(R)-1-(p-Tolyl)-1,2,2-trimethylcyclopentane

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About This Item

Empirical Formula (Hill Notation):
C15H22
CAS Number:
Molecular Weight:
202.34
Beilstein/REAXYS Number:
2326949
EC Number:
MDL number:
UNSPSC Code:
12352002
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

≥99.0% (sum of enantiomers, GC)

optical activity

[α]20/D +64±2°, neat

refractive index

n20/D 1.523

bp

275 °C (lit.)

density

0.937 g/mL at 20 °C (lit.)

storage temp.

2-8°C

SMILES string

Cc1ccc(cc1)[C@]2(C)CCCC2(C)C

InChI

1S/C15H22/c1-12-6-8-13(9-7-12)15(4)11-5-10-14(15,2)3/h6-9H,5,10-11H2,1-4H3/t15-/m0/s1

InChI key

SLKPBCXNFNIJSV-HNNXBMFYSA-N

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Acute Tox. 4 Oral

Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


Certificates of Analysis (COA)

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María Peñuelas et al.
The Plant cell, 31(10), 2491-2509 (2019-08-09)
The lipid-derived phytohormone jasmonoyl-isoleucine regulates plant immunity, growth and development in vascular plants by activating genome-wide transcriptional reprogramming. In Arabidopsis (Arabidopsis thaliana), this process is largely orchestrated by the master regulator MYC2 and related transcription factors (TFs). However, the TFs

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