16571

(+)-3-Brom-campher

purum, ≥97.0% (sum of enantiomers, GC)

• Synonym(e): endo-(1R)-3-Brom-1,7,7-trimethylbicyclo[2.2.1]heptan-2-on
• Empirische Formel (Hill-System): C₁₀H₁₅BrO
• CAS-Nummer: 10293-06-8
• Molekulargewicht: 231.13
• Beilstein: 3197237
• EG-Nummer: 233-652-1
• MDL-Nummer: MFCD00003744
• UNSPSC-Code: 12352115
• PubChem Substanz-ID: 57647579
• NACRES: NA.22

Eigenschaften

• Qualität: purum
• Qualitätsniveau: 200
• Assay: ≥97.0% (sum of enantiomers, GC)
• Form: solid
• Optische Aktivität: [α]20/D +136±3°, c = 1% in ethanol
• mp (Schmelzpunkt): 75-77 °C
• Funktionelle Gruppe: bromo; ketone
• SMILES String: [H][C@@]12CC[C@@](C)(C(=O)[C@H]1Br)C2(C)C
• InChI: 1S/C10H15BrO/c1-9(2)6-4-5-10(9,3)8(12)7(6)11/h6-7H,4-5H2,1-3H3/t6-,7+,10+/m1/s1
• InChIKey: NJQADTYRAYFBJN-FWWHASMVSA-N

Beschreibung

Anwendung

• Insights into the mechanisms of within-species variation in sensitivity to chemicals: A case study using daphnids exposed to CMIT/MIT biocide.: This study investigates the differential sensitivity of daphnids to 2-Methyl-4-isothiazolin-3-one, highlighting the biochemical mechanisms underlying these variations. The findings provide crucial insights for environmental safety assessments (Kim et al., 2023).

Sonstige Hinweise

Use as chiral building block; Debromo-silylation and -phosphonylation

Sicherheitshinweise

• Piktogramme: GHS07
• Signalwort: Warning
• H-Sätze: H315,H319,H335
• P-Sätze: P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338
• Gefahreneinstufungen: Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
• Zielorgane: Respiratory system
• Lagerklassenschlüssel: 11 - Combustible Solids
• WGK: WGK 3
• Flammpunkt (°F): Not applicable
• Flammpunkt (°C): Not applicable
• Persönliche Schutzausrüstung: dust mask type N95 (US), Eyeshields, Gloves