232386
(+)-2-Carene
97%
동의어(들):
(1S)-3,7,7-Trimethylbicyclo[4.1.0]hept-2-ene
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크기 선택
제품정보 (DICE 배송 시 비용 별도)
실험식(Hill 표기법):
C10H16
CAS 번호:
Molecular Weight:
136.23
UNSPSC Code:
12352002
NACRES:
NA.22
PubChem Substance ID:
EC Number:
224-792-4
Beilstein/REAXYS Number:
2038651
MDL number:
Assay:
97%
Quality Level
assay
97%
optical activity
[α]20/D +90.0°, c = 6 in ethanol
refractive index
n20/D 1.476 (lit.)
bp
167-168 °C (lit.)
density
0.862 g/mL at 25 °C (lit.)
SMILES string
CC1=C[C@H]2[C@@H](CC1)C2(C)C
InChI
1S/C10H16/c1-7-4-5-8-9(6-7)10(8,2)3/h6,8-9H,4-5H2,1-3H3/t8-,9+/m1/s1
InChI key
IBVJWOMJGCHRRW-BDAKNGLRSA-N
General description
(+)-2-Carene is a natural bicyclic monoterpene that is commonly found in the essential oils of various plants, such as rosemary, cedarwood, and pine. In organic synthesis, it is used as a chiral building block for the synthesis of a variety of chiral compounds.
Application
(+)-2-Carene can be used as a chiral building block in the synthesis of chiral non-racemic 2,2-dimethyl-1,3-disubstituted cyclopropane derivatives. It is also used as a reactant in the enantio-selective synthesis of (+)-α-elemene.
Codruta Ignea et al.
Nature communications, 10(1), 3799-3799 (2019-08-25)
Synthetic biology efforts for the production of valuable chemicals are frequently hindered by the structure and regulation of the native metabolic pathways of the chassis. This is particularly evident in the case of monoterpenoid production in Saccharomyces cerevisiae, where the
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