Search Thermo Fisher Scientific
Element Search
Structure Search
Thermo Scientific Chemicals
2-Naphthaldehyde, 98%, Thermo Scientific Chemicals
Have Questions?
Change view
Catalog number B25157.06
also known as B25157-06
Price (USD)/ Each
53.00
-
Quantity:
5 g
Price (USD)/ Each
53.00
2-Naphthaldehyde, 98%, Thermo Scientific Chemicals
Catalog numberB25157.06
Price (USD)/ Each
53.00
-
Chemical Identifiers
CAS66-99-9
IUPAC Namenaphthalene-2-carbaldehyde
Molecular FormulaC11H8O
InChI KeyPJKVFARRVXDXAD-UHFFFAOYSA-N
SMILESO=CC1=CC=C2C=CC=CC2=C1
View more
Specifications
Specification Sheet
Specification SheetAppearance (Color)White to cream
FormCrystals or powder or crystalline powder or lumps
Assay (GC)≥97.5%
Free acid (titration)≤1%
Identification (FTIR)Conforms
View more
2-Naphthaldehyde aids in stereo-selective formation of bicyclo 2-siloxy-2-alkoxyoxetanes. It is also used as catalytic agent and petrochemical additive.
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
2-Naphthaldehyde aids in stereo-selective formation of bicyclo 2-siloxy-2-alkoxyoxetanes. It is also used as catalytic agent and petrochemical additive.
Solubility
Soluble in hot water.
Notes
Store at -20°C. Air Sensitive. Store away from string bases and oxidizing agents.
2-Naphthaldehyde aids in stereo-selective formation of bicyclo 2-siloxy-2-alkoxyoxetanes. It is also used as catalytic agent and petrochemical additive.
Solubility
Soluble in hot water.
Notes
Store at -20°C. Air Sensitive. Store away from string bases and oxidizing agents.
RUO – Research Use Only
General References:
- K Wichmann; T Krusius; R Sinervirta; J Puranen; J Jänne. Studies on structure-activity relationship of gossypol, gossypol ethers and three naphthaldehydes in the inhibition of spermatozoal metabolism. Contraception.1986, 33, (5), 519-528.
- Manabu Abe; Masayuki Ikeda; Yasuo Shirodai; Masatomo Nojima. Regio- and stereo-selective formation of 2-siloxy-2-alkoxyoxetanes in the photoreaction of cyclic ketene silyl acetals with 2-naphthaldehyde and their transformation to aldol-type adducts. Tetrahedron Letters.1996, 37, 5901-5904.