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Dokumente

115576

Sigma-Aldrich

3-Caren

90%

Synonym(e):

δ3-Caren, 3,7,7-Trimethyl-bicyclo[4.1.0]hept-3-en

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About This Item

Empirische Formel (Hill-System):
C10H16
CAS-Nummer:
13466-78-9
Molekulargewicht:
136.23
EG-Nummer:
236-719-3
MDL-Nummer:
MFCD00001315
UNSPSC-Code:
12352212
PubChem Substanz-ID:
24847227
NACRES:
NA.22

Assay

90%

Optische Aktivität

[α]20/D +15°, neat

Verunreinigungen

5% 2-carene

Brechungsindex

n20/D 1.474 (lit.)

bp

168-169 °C/705 mmHg (lit.)

Dichte

0.857 g/mL at 25 °C (lit.)

SMILES String

CC1=CCC2C(C1)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

InChIKey

BQOFWKZOCNGFEC-UHFFFAOYSA-N

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Signalwort

Danger

Gefahreneinstufungen

Aquatic Chronic 3 - Asp. Tox. 1 - Flam. Liq. 3 - Skin Irrit. 2 - Skin Sens. 1

Lagerklassenschlüssel

3 - Flammable liquids

WGK

WGK 2

Flammpunkt (°F)

116.6 °F - closed cup

Flammpunkt (°C)

47 °C - closed cup

Persönliche Schutzausrüstung

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

Analysenzertifikate (COA)

Suchen Sie nach Analysenzertifikate (COA), indem Sie die Lot-/Chargennummer des Produkts eingeben. Lot- und Chargennummern sind auf dem Produktetikett hinter den Wörtern ‘Lot’ oder ‘Batch’ (Lot oder Charge) zu finden.

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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Min Lu et al.
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Novel genotypes often arise during biological invasions, but their role in invasion success has rarely been elucidated. Here we examined the population genetics and behavior of the fungus, Leptographium procerum, vectored by a highly invasive bark beetle, Dendroctonus valens, to
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Marie Danielsson et al.
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Norway spruce [Picea abies (L.) Karst.] is one of the most important conifer species in Europe. The wood is economically important and infections by wood-rotting fungi cause substantial losses to the industry.The first line of defence in a Norway spruce
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A novel carene-based alanine-equivalent tricyclic iminolactone 16 has been synthesized via stereoselective dihydroxylation of the double bond, IBX oxidation of the secondary alcohol, esterification of the tertiary alcohol, deprotection of the resulting ester, and subsequent cyclization from commercially available (1S)-(+)-3-carene
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