467030
1-Cyclohexene-1-carboxaldehyde
97%
Synonym(s):
Δ1-Tetrahydrobenzaldehyde, 1-Cyclohexenecarboxaldehyde, 1-Cyclohexenylaldehyde, 1-Formyl-1-cyclohexene, 1-Formylcyclohexene
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About This Item
Linear Formula:
C6H9CHO
CAS Number:
Molecular Weight:
110.15
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Quality Level
assay
97%
bp
61 °C/10 mmHg (lit.)
density
0.966 g/mL at 25 °C (lit.)
functional group
aldehyde
SMILES string
O=CC1=CCCCC1
InChI
1S/C7H10O/c8-6-7-4-2-1-3-5-7/h4,6H,1-3,5H2
InChI key
OANSOJSBHVENEI-UHFFFAOYSA-N
General description
1-Cyclohexene-1-carboxaldehyde is an α,β-unsaturated aldehyde. It participates in the synthesis of benzopyrans.
Application
1-Cyclohexene-1-carboxaldehyde may be used in the synthesis of azomethine imines.
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
149.0 °F - closed cup
flash_point_c
65 °C - closed cup
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Environmentally benign, one-pot synthesis of pyrans by domino Knoevenagel/6p-electrocyclization in water and application to natural products.
Jung EJ, et al.
Green Chemistry, 12(11), 2003-2011 (2010)
Feng Shi et al.
Tetrahedron letters, 50(28), 4067-4070 (2010-02-18)
A [3+2] 1,3-dipolar cycloaddition reaction of arynes with stable azomethine imines has been developed. The reaction rapidly assembles tricyclic pyrazoloindazolone derivatives in moderate yields under mild reaction conditions.
Efficient and general method for the synthesis of benzopyrans by ethylenediamine diacetate-catalyzed reactions of resorcinols with α, β-unsaturated aldehydes. One step synthesis of biologically active (?)-confluentin and (?)-daurichromenic acid.
Lee YR, et al.
Tetrahedron Letters, 46(44), 7539-7543 (2005)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| M8449-10UG | 04061833247495 |
| 467030-1G | 04061837500077 |
| 467030-5G | 04061837500084 |