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1-(Bromomethyl)naphthalene, 98%, Thermo Scientific Chemicals
| Catalog Number | Quantity |
|---|---|
| ALFH64116.14 | 25 g |
Catalog number ALFH64116.14
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Quantity:
25 g
Chemical Identifiers
CAS7440-36-0
IUPAC Nameantimony
Molecular FormulaSb
InChI KeyWATWJIUSRGPENY-UHFFFAOYSA-N
SMILES[Sb]
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Specifications
Specification Sheet
Specification SheetTotal Metal Impurities0.001% max.
It is employed as a intermediate for organic synthesis and pharmaceutical.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
It is employed as a intermediate for organic synthesis and pharmaceutical.
Solubility
Slightly soluble in water.
Notes
Refrigerate. Keep container tightly closed. Store away from oxidizing agent.
It is employed as a intermediate for organic synthesis and pharmaceutical.
Solubility
Slightly soluble in water.
Notes
Refrigerate. Keep container tightly closed. Store away from oxidizing agent.
RUO – Research Use Only
General References:
- Linda J. Johnston; J. C. Scaiano. Generation, spectroscopy, and reactivity of excited 1-naphthylmethyl radicals. Org. Lett. 1985107(22), 6368-6372.
- Takashi Ooi; Yuichiro Arimura; Yukihiro Hiraiwa; Lin Ming Yuan; Taichi Kano; Toru Inoue; Jun Matsumoto; Keiji Maruoka. Highly enantioselective monoalkylation of p-chlorobenzaldehyde imine of glycine tert-butyl ester under mild phase-transfer conditions. Tetrahedron: Asymmetry. 200617(4), 603-606.