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About This Item
Empirical Formula (Hill Notation):
C10H7Br
CAS Number:
Molecular Weight:
207.07
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-452-5
Beilstein/REAXYS Number:
1858110
MDL number:
Assay:
97%
Form:
solid
Quality Level
assay
97%
form
solid
impurities
≤3% 1-bromonaphthalene
bp
281-282 °C (lit.)
mp
52-55 °C (lit.)
solubility
methanol: soluble 50 mg/mL, clear, colorless to yellow
functional group
bromo
SMILES string
Brc1ccc2ccccc2c1
InChI
1S/C10H7Br/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7H
InChI key
APSMUYYLXZULMS-UHFFFAOYSA-N
Gene Information
human ... CYP2A6(1548)
mouse ... Cyp2a5(13087)
General description
Reaction of 2-bromonaphthalene with cuprous cyanide in N-methylpyrrolidone has been investigated. Nanosecond time-resolved resonance Raman spectra of the T1→Tn transition of 2-bromonaphthalene in methanol solvent has been investigated.
Application
2-Bromonaphthalene was used in the synthesis of biaryls via Suzuki cross coupling reaction in water under microwave irradiation.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Rapid microwave-promoted Suzuki cross coupling reaction in water.
Bai L, et al.
Green Chemistry, 5(5), 615-617 (2003)
Nanosecond time-resolved resonance Raman investigation of the T1→ Tn transition of 2-bromonaphthalene.
Shoute LCT, et al.
Chemical Physics Letters, 290(1), 24-28 (1998)
Notes-A Convenient Synthesis of Water-Soluble Carbodiimides.
Sheehan J, et al.
The Journal of Organic Chemistry, 26(7), 2525-2528 (1961)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 183644-5G | 04061838756282 |
| 183644-25G | 04061838346674 |
