Cas 119476-25-4,(2,5-dihydrofuran-3-yl)(phenyl)methanone

119476-25-4

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Basic information

Product Name: (2,5-dihydrofuran-3-yl)(phenyl)methanone
Synonyms: (2,5-dihydrofuran-3-yl)(phenyl)methanone
CAS NO:119476-25-4
Molecular Formula:
Molecular Weight: 174.199
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (2,5-dihydrofuran-3-yl)(phenyl)methanone(CAS DataBase Reference)
NIST Chemistry Reference: (2,5-dihydrofuran-3-yl)(phenyl)methanone(119476-25-4)
EPA Substance Registry System: (2,5-dihydrofuran-3-yl)(phenyl)methanone(119476-25-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 119476-25-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 119476-25-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,4,7 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 119476-25:
(8*1)+(7*1)+(6*9)+(5*4)+(4*7)+(3*6)+(2*2)+(1*5)=144
144 % 10 = 4
So 119476-25-4 is a valid CAS Registry Number.

119476-25-4Upstream product

119476-25-4Downstream Products

119476-25-4Relevant academic research and scientific papers

Iron(III)-catalyzed cyclization of alkynyl aldehyde acetals: Experimental and computational studies

Xu, Tongyu,Yang, Qin,Li, Dongpo,Dong, Jinhua,Yu, Zhengkun,Li, Yuxue

supporting information; experimental part, p. 9264 - 9272 (2010/10/03)

FeCl3·6H2O-and FeBr3-catalyzed Prins cyclization/halogenation of alkynyl aldehyde acetals has been realized with acetyl chloride or bromide as halogen source in dichloromethane to afford 2-(1-halobenzylidene or alkylidene)

Indium(III)-catalyzed coupling between alkynes and aldehydes to α,β-unsaturated ketones

Miura, Katsukiyo,Yamamoto, Kiyomi,Yamanobe, Aya,Ito, Keisuke,Kinoshita, Hidenori,Ichikawa, Junji,Hosomi, Akira

, p. 766 - 767 (2011/01/09)

The combined use of a catalytic amount of InX3 (X = OTf and NTf2) and 1-butanol was found to be effective in formal alkynealdehyde metathesis. With this catalytic system, aromatic alkynes reacted with aromatic aldehydes to give chalcones in moderate to good yields. Alkynals were efficiently converted into 5- to 7-membered cyclic compounds by intramolecular alkyne-aldehyde coupling.

Alkynes as synthetic equivalents to stabilized wittig reagents: Intra- and intermolecular carbonyl olefinations catalyzed by Ag(I), BF3, and HBF4

Rhee, Jong Uk,Krische, Michael J.

, p. 2493 - 2495 (2007/10/03)

(Chemical Equation Presented) The first use of cationic silver (AgSbF 4) as a catalyst for intra- and intermolecular alkyne - carbonyl coupling to form conjugated enones is described, and a comparison to corresponding Bronsted acid (HBF4/

REACTION OF TETRAHYDROFUROISOXAZOLES WITH MOLYBDENUM HEXACARBONYL. A NEW ROUTE TO PREPARATION OF 3-SUBSTITUTED TETRAHYDRO- AND DIHYDROFURAN DERIVATIVES

Fisera, Lubor,Goljer, Igor,Jaroskova, Libuse

, p. 1753 - 1760 (2007/10/02)

3-(4-X-Phenyl)-3a,4,6,6a-tetrahydrofuroisoxazoles Ia-If (X = H, CH3, CH3O, Cl, F, C6H5) react with molybdenum hexacarbonyl to give not only the expected cis-3-aroyl-4-hydroxytetrahydrofuran III, but also its trans isomer IV and 3-aroyl-2,5-dihydrof

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