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Cyclopropanecarboxaldehyde

  • CAS:1489-69-6
  • purity:99%
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Manufacturer supply high quality Cyclopropanecarboxaldehyde 1489-69-6 with GMP standards

  • Molecular Formula: C4H6O
  • Molecular Weight: 70.091
  • Appearance/Colour: Clear colorless liquid 
  • Vapor Pressure: 38.2mmHg at 25°C 
  • Refractive Index: n20/D 1.4298(lit.)  
  • Boiling Point: 99.5 °C at 760 mmHg 
  • Flash Point: 7.2 °C 
  • PSA: 17.07000 
  • Density: 1.171 g/cm3 
  • LogP: 0.59530 

Cyclopropanecarboxaldehyde(Cas 1489-69-6) Usage

Preparation

Cyclopropanecarboxaldehyde is prepared by reaction of cyclopropylmethanol. The reaction needs reagent pyridinium chlorochromate and solvent CH2Cl2 with other condition of ambient temperature for 3 hours. The yield is about 60%.

Application

Cyclopropanecarboxaldehyde is a reagent in the preparation of N-alkylphenylalaninamides of pyridinylphenyland oxobipyridinylamines as human GPR 142 agonists for potential use as anti-diabetic agents and the cytochrome P 450 inhibition.

InChI:InChI=1/C4H6O/c5-3-4-1-2-4/h3-4H,1-2H2

1489-69-6 Relevant articles

Microstructured Au/Ni-fiber catalyst: Galvanic reaction preparation and catalytic performance for low-temperature gas-phase alcohol oxidation

Zhao, Guofeng,Deng, Miaomiao,Jiang, Yifeng,Hu, Huanyun,Huang, Jun,Lu, Yong

, p. 46 - 53 (2013)

The highly active and selective gold cat...

Practical Os/Cu-cocatalyzed air oxidation of allyl and benzyl alcohols at room temperature and atmospheric pressure

Muldoon, John,Brown, Seth N.

, p. 1043 - 1045 (2002)

(equation presented) A new protocol for ...

Cyclopropanation of Electron-deficient Olefins with Dibromomethane by Ni(0) Complexes and Zinc

Kanai, Hiroyoshi,Hiraki, Nobuyuki,Iida, Shigeki

, p. 1025 - 1029 (1983)

A new method for the synthesis of cyclop...

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Wiberg,Lavanish

, p. 5272 (1966)

-

Scope, Limitation, and Mechanism of the Homoconjugate Electrophilic Addition of Hydrogen Halides

Lambert, Joseph B.,Napoli, James J.,Johnson, Katharine Kappauf,Taba, Kalulu N.,Packard, Beverly Sue

, p. 1291 - 1295 (1985)

Hydrogen halides (HCl, HBr, HI) add by a...

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Roberts

, p. 2959 (1951)

-

Cu3Pt1-Cu2O nanocomposites: Synergistic effect-dependent high activity and stability for the gas-phase selective oxidation of alcohols

Liu, Kun,Long, Houkun,Wang, Guangyi,Sun, Yongbin,Hou, Chao,Dong, Jian,Cao, Xiaoqun

, p. 54861 - 54865 (2017)

The catalyst Cu3Pt1-Cu2O/SiC was facilel...

ELECTROCHEMICAL AND CHEMICAL OXIDATION OF ALCOHOLS IN A TWO-PHASE SYSTEM USING N-OXOPIPERIDINUM SALT: SYNTHESIS OF 4-CHLOROBUTANAL, FORMYLCYCLOPROPANES, AND m-PHENOXYBENZALDEHYDE

Ogibin, Yu. N.,Khusid, A. Kh.,Nikishin, G. I.

, p. 735 - 739 (1992)

Oxidation of 4-chlorobutanol-1, cyclopro...

Short-lived 1,5-biradicals formed from triplet 1-alkoxy- and 1-(benzyloxy)-9,10-anthraquinones

Smart, Robert P.,Peelen, Timothy J.,Blankespoor, Ronald L.,Ward, Donald L.

, p. 461 - 465 (1997)

The cyclopropylmethyl and (trans-2-pheny...

Oxetane ring enlargement through nucleophilic trapping of radical cations by acetonitrile

Perez-Ruiz, Raul,Saez, Jose A.,Domingo, Luis R.,Jimenez, M. Consuelo,Miranda, Miguel A.

, p. 5700 - 5703 (2012)

Oxidative electron transfer cycloreversi...

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Smith,Rogier

, p. 4047 (1951)

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Kinetics of Cyclopentene Isomerization at 1200 K

Lewis, David K.,Baldwin, John E.,Cianciosi, Steven J.

, p. 7464 - 7467 (1990)

This study was conducted to determine th...

Method for synthesizing cyclopropanecarboxaldehyde from 1,4-butanediol

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Paragraph 0054-0058; 0064-0068, (2021/03/13)

The invention relates to a method for sy...

Flavin Nitroalkane Oxidase Mimics Compatibility with NOx/TEMPO Catalysis: Aerobic Oxidization of Alcohols, Diols, and Ethers

Thapa, Pawan,Hazoor, Shan,Chouhan, Bikash,Vuong, Thanh Thuy,Foss, Frank W.

, p. 9096 - 9105 (2020/08/14)

Biomimetic flavin organocatalysts oxidiz...

Thiourea-Mediated Halogenation of Alcohols

Mohite, Amar R.,Phatake, Ravindra S.,Dubey, Pooja,Agbaria, Mohamed,Shames, Alexander I.,Lemcoff, N. Gabriel,Reany, Ofer

, p. 12901 - 12911 (2020/11/26)

The halogenation of alcohols under mild ...

Novel method for synthesizing cyclopropyl formaldehyde

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Paragraph 0008; 0013; 0016, (2020/09/09)

The invention relates to a novel method ...

1489-69-6 Process route

(E)-4-chlorobut-2-enal
31930-38-8

(E)-4-chlorobut-2-enal

4-chlorobutyraldehyde
6139-84-0

4-chlorobutyraldehyde

Cyclopropanecarboxaldehyde
1489-69-6

Cyclopropanecarboxaldehyde

Conditions
Conditions Yield
With wild-type 12-oxophytodienoicacid reductase 3 from Solanum lycopersicum Y190F mutant; NADH; In aq. phosphate buffer; N,N-dimethyl-formamide; at 25 ℃; for 3h; pH=7.5; Reagent/catalyst; Darkness; Inert atmosphere; Schlenk technique; Enzymatic reaction;
cyclopropylmethyl benzoylformate

cyclopropylmethyl benzoylformate

benzaldehyde
100-52-7

benzaldehyde

3-hydroxy-3-phenylcycloheptene-6-lactone

3-hydroxy-3-phenylcycloheptene-6-lactone

Cyclopropanecarboxaldehyde
1489-69-6

Cyclopropanecarboxaldehyde

Conditions
Conditions Yield
In benzene; Quantum yield; Irradiation;
In benzene; Irradiation;

1489-69-6 Upstream products

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    ethyl tetrahydrofurancarboxylate

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    14372-24-8

    cyclopropyl(piperidin-1-yl)methanone

1489-69-6 Downstream products

  • 582299-31-8
    582299-31-8

    (E)-3-cyclopropyl-1-phenylprop-2-en-1-one

  • 71056-31-0
    71056-31-0

    cyclopropanecarbaldehyde phenylhydrazone

  • 36873-36-6
    36873-36-6

    1-(cyclopropylmethylene)-2-(2,4-dinitrophenyl)hydrazine

  • 60129-33-1
    60129-33-1

    (trans)-3-cyclopropylacrylic acid

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