Cyclopropanecarboxyldehyde

Modify Date: 2025-08-23 17:34:54

Cyclopropanecarboxyldehyde Structure
Cyclopropanecarboxyldehyde structure
Common Name Cyclopropanecarboxyldehyde
CAS Number 1489-69-6 Molecular Weight 70.090
Density 1.2±0.1 g/cm3 Boiling Point 99.5±0.0 °C at 760 mmHg
Molecular Formula C4H6O Melting Point N/A
MSDS Chinese USA Flash Point 7.2±0.0 °C
Symbol GHS02 GHS05
GHS02, GHS05
Signal Word Danger

 Names

Name Cyclopropanecarboxaldehyde
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.2±0.1 g/cm3
Boiling Point 99.5±0.0 °C at 760 mmHg
Molecular Formula C4H6O
Molecular Weight 70.090
Flash Point 7.2±0.0 °C
Exact Mass 70.041862
PSA 17.07000
LogP 0.21
Vapour Pressure 38.2±0.1 mmHg at 25°C
Index of Refraction 1.599
Storage condition Refrigerator

 Safety Information

Symbol GHS02 GHS05
GHS02, GHS05
Signal Word Danger
Hazard Statements H225-H314
Precautionary Statements P210-P280-P305 + P351 + P338-P310
Personal Protective Equipment Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
Hazard Codes F:Flammable;C:Corrosive;
Risk Phrases R11;R34
Safety Phrases S16-S26-S36/37/39-S45
RIDADR UN 2924 3/PG 2
WGK Germany 3
RTECS GZ1005000
Packaging Group II
Hazard Class 3
HS Code 2912299000

 Synthetic Route

 Customs

HS Code 2912299000
Summary 2912299000. other cyclic aldehydes without other oxygen function. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:5.5%. General tariff:30.0%

 Articles4

More Articles
Synthesis and reactivity of six-membered oxa-nickelacycles: a ring-opening reaction of cyclopropyl ketones.

Chemistry 15(39) , 10083-91, (2009)

Cyclopropanecarboxaldehyde (1 a), cyclopropyl methyl ketone (1 b), and cyclopropyl phenyl ketone (1 c) were reacted with [Ni(cod)(2)] (cod = 1,5-cyclooctadiene) and PBu(3) at 100 degrees C to give eta...

Wang, Z. et al

Tetrahedron Lett. 41 , 4007, (2000)

Palladium-catalyzed asymmetric [3 + 2] trimethylenemethane cycloaddition reactions.

J. Am. Chem. Soc. 128 , 13328, (2006)

Transition-metal-catalyzed trimethylenemethane (TMM) [3 + 2] cycloadditions provide direct routes to functionalized cyclopentanes. This reaction has been shown to be a highly chemo-, regio-, and diast...

 Synonyms

Cyclopropanecarboxaldehyde
MFCD00012261
Cyclopropanecarbaldehyde
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