441619

(1S)-(+)-3-Carene

99%

• 동의어(들): (+)-3-Carene, (1S)-3,7,7-Trimethylbicyclo[4.1.0]hept-3-ene
• 실험식(Hill 표기법): C₁₀H₁₆
• CAS Number: 498-15-7
• Molecular Weight: 136.23
• Beilstein: 1902767
• EC Number: 207-856-6
• MDL number: MFCD00066417
• UNSPSC 코드: 12352205
• PubChem Substance ID: 24867688
• NACRES: NA.22

속성

• 분석: 99%
• 형태: liquid
• 광학 활성: [α]20/D +17°, neat
• refractive index: n20/D 1.472 (lit.)
• bp: 170-172 °C (lit.)
• density: 0.865 g/mL at 25 °C (lit.)
• SMILES string: [H][C@@]12CC=C(C)C[C@]1([H])C2(C)C
• InChI: 1S/C10H16/c1-7-4-5-8-9(6-7)10(8,2)3/h4,8-9H,5-6H2,1-3H3/t8-,9+/m1/s1
• InChI key: BQOFWKZOCNGFEC-BDAKNGLRSA-N

설명

일반 설명

(1S)-(+)-3-Carene is a monoterpene.

애플리케이션

(1S)-(+)-3-Carene has been used as a standard during the quantification of components in Lavandula stoechas essential oils by fast gas chromatography-mass spectrometry (FGC-EI/MS). It may be used as a starting material in the total synthesis of (+)-ingenol. It may also be used to synthesize (1S,3S,4S,6R)-3,7,7-trimethyl-4-morpholino-4-yl-bicyclo(4.1.0)heptano-3-ol, which can catalyze the addition of diethylzinc to different aldehydes with high enantioselectivity.

Chiral building block for the preparation of bicyclo[3.2.0]heptenes that are useful intermediates in the synthesis of (+)-lineatin and both enantiomers of capnellene. Has been converted to its corresponding allenyl allylic ether for studies of its thermal isomerization chemistry. Precursor to di(4-isocaranyl)borane, an asymmetric hydroboration reagent for olefins.

안전성 정보

• 픽토그램: GHS02,GHS08,GHS07,GHS09
• 신호어: Danger
• 유해 및 위험 성명서: H226,H304,H315,H317,H410
• 예방조치 성명서: P210 - P273 - P280 - P301 + P310 - P303 + P361 + P353 - P331
• Hazard Classifications: Aquatic Acute 1 - Aquatic Chronic 1 - Asp. Tox. 1 - Flam. Liq. 3 - Skin Irrit. 2 - Skin Sens. 1
• Storage Class Code: 3 - Flammable liquids
• WGK: WGK 3
• Flash Point (°F): 116.6 °F - closed cup
• Flash Point (°C): 47 °C - closed cup
• 개인 보호 장비: Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter