| Weight | 136.238 g/mol |
|---|---|
| Formula | C10H16 |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
(+)-3-Carene (498-15-7, 13466-78-9)
3-carene, (R)-isomer · 3-carene · 3-carene, (S)-(cis)-isomer
Score:
#1618 in Physics
,
#3944 in Biology
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#4963 in Chemistry
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- Sigma-Aldrich - (+)-3-Carene46.70 - 361.50 USD
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- Traumatic resin defense in Norway spruce (Picea abies): methyl jasmonate-induced terpene synthase gene expression, and cDNA cloning and functional characterization of (+)-3-carene synthase. (Plant Molecular Biology, 2003)
- 14-Step Synthesis of (+)-Ingenol from (+)-3-Carene (Science, 2013)
- An Efficient Chiral Moderator Prepared from Inexpensive (+)-3-Carene: Synthesis of the HIV-1 Non-Nucleoside Reverse Transcriptase Inhibitor DPC 963 (Organic Letters, 2000)
- Kinetics of the gas-phase reactions of OH and NO sub 3 radicals with 2-carene, 1,8-cineole, p-cymene, and terpinolene (Environmental Science & Technology, 1990)
- An integrated genomic, proteomic and biochemical analysis of (+)3carene biosynthesis in Sitka spruce (Picea sitchensis) genotypes that are resistant or susceptible to white pine weevil (Plant Journal, 2011)
- Terpenoids Biotransformation in Mammals III: Biotransformation of -Pinene, -Pinene, Pinane, 3-Carene, Carane, Myrcene, and p-Cymene in Rabbits (Journal of Pharmaceutical Sciences, 1981)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3-carene, (R)-isomer
- 3-carene
- 3-carene, (S)-(cis)-isomer
-
SMILESCC1=CCC2C(C1)C2(C)C
-
InChIKeyBQOFWKZOCNGFEC-UHFFFAOYSA-N
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(+)-3-Carene
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