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Cinnamyl chloride, 95%, stab. with sodium carbonate
CAS: 2687-12-9 | C9H9Cl | 152.62 g/mol
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Catalog number A14408.30
also known as A14408-30
Price (USD)
204.65
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Quantity:
250 g
Price (USD)
204.65
Online Exclusive
227.00Save 22.35 (10%)
Each
Chemical Identifiers
CAS2687-12-9
IUPAC Name[(1E)-3-chloroprop-1-en-1-yl]benzene
Molecular FormulaC9H9Cl
InChI KeyIWTYTFSSTWXZFU-QPJJXVBHSA-N
SMILESClC\C=C\C1=CC=CC=C1
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Specifications
Specification Sheet
Specification SheetAppearance (Color)Clear colorless to yellow to yellow-brown
Identification (FTIR)Conforms
Refractive Index1.5810-1.5870 @ 20?C
Assay (GC)≥94.0%
FormLiquid
Cinnamyl chloride is used in the enantioselective total synthesis of helioporins C and E, bioactive marine diterpenes.
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
Cinnamyl chloride is used in the enantioselective total synthesis of helioporins C and E, bioactive marine diterpenes.
Solubility
Soluble in water (0.2 g/L at 20°C).
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Containers which are opened must be carefully resealed and kept upright to prevent leakage. Recommended storage temperature: 2 - 8°C
Cinnamyl chloride is used in the enantioselective total synthesis of helioporins C and E, bioactive marine diterpenes.
Solubility
Soluble in water (0.2 g/L at 20°C).
Notes
Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Containers which are opened must be carefully resealed and kept upright to prevent leakage. Recommended storage temperature: 2 - 8°C
RUO – Research Use Only
General References:
- Kenji Uneyama.; Hiromi Nanbu.; Sigeru Torii. Reductive generation of active zero-valent in SnCl2Al system and its use for highly diastereoselective reaction of cinnamyl chloride and aldehydes. Tetrahedron Letters. 1986, 27 (21), 2395-2396.
- Henry Gilman andStanton A. Harris. The preparation of cinnamyl chloride and its grignard reagent. Recueil des Travaux Chimiques des Pays-Bas. 1931, 50 (12), 1052-1055.