What is the (E)-5-(phenylmethylene)furan-2(5H)-one?

(E)-5-(phenylmethylene)furan-2(5H)-one is , while it's Molecular Formula is C11H8 O2. Used in Pharmaceutical and Agrochemical Industries: (E)-5-(phenylmethylene)furan-2(5H)-one is utilized as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its distinctive structure allows for the development of novel compounds with potential applications in these fields. Used in Research and Development: (E)-5-(phenylmethylene)furan-2(5H)-one is also employed in research and development, where it is studied for its potential biological activities and implications in drug development. The exploration of its properties and interactions with other molecules contributes to the advancement of chemistry and pharmacology. Used in Chemical Synthesis: (E)-5-(phenylmethylene)furan-2(5H)-one serves as a valuable building block in chemical synthesis, enabling the creation of a wide range of compounds with diverse applications across various industries. Its unique properties make it a promising candidate for the development of new products with commercial and scientific potential.

What is the CAS number for (E)-5-(phenylmethylene)furan-2(5H)-one?

The CAS number of (E)-5-(phenylmethylene)furan-2(5H)-one is 35304-87-1.

What is (E)-5-(phenylmethylene)furan-2(5H)-one (35304-87-1) used for?

(E)-5-(phenylmethylene)furan-2(5H)-one, with the molecular formula C12H8O2, is a yellow crystalline solid that is recognized for its aromatic and fruity odor. This chemical compound is valued for its unique structure and properties, which make it a versatile building block in the creation of new and diverse compounds with potential commercial and scientific utility.

What is the (E)-5-(phenylmethylene)furan-2(5H)-one?

(E)-5-(phenylmethylene)furan-2(5H)-one is , while it's Molecular Formula is C11H8 O2. Used in Pharmaceutical and Agrochemical Industries: (E)-5-(phenylmethylene)furan-2(5H)-one is utilized as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its distinctive structure allows for the development of novel compounds with potential applications in these fields. Used in Research and Development: (E)-5-(phenylmethylene)furan-2(5H)-one is also employed in research and development, where it is studied for its potential biological activities and implications in drug development. The exploration of its properties and interactions with other molecules contributes to the advancement of chemistry and pharmacology. Used in Chemical Synthesis: (E)-5-(phenylmethylene)furan-2(5H)-one serves as a valuable building block in chemical synthesis, enabling the creation of a wide range of compounds with diverse applications across various industries. Its unique properties make it a promising candidate for the development of new products with commercial and scientific potential.

What is the CAS number for (E)-5-(phenylmethylene)furan-2(5H)-one?

The CAS number of (E)-5-(phenylmethylene)furan-2(5H)-one is 35304-87-1.

What is (E)-5-(phenylmethylene)furan-2(5H)-one (35304-87-1) used for?

(E)-5-(phenylmethylene)furan-2(5H)-one, with the molecular formula C12H8O2, is a yellow crystalline solid that is recognized for its aromatic and fruity odor. This chemical compound is valued for its unique structure and properties, which make it a versatile building block in the creation of new and diverse compounds with potential commercial and scientific utility.

(E)-5-(phenylmethylene)furan-2(5H)-one

Base Information

Chemical Name: (E)-5-(phenylmethylene)furan-2(5H)-one
CAS No.: 35304-87-1

Chinese Manufacturer Supply (E)-5-(phenylmethylene)furan-2(5H)-one 35304-87-1 On Stock with Competitive Price

Molecular Formula: C11H8 O2
Molecular Weight: 172.183
Boiling Point: 349.9°Cat760mmHg
Flash Point: 145.8°C
PSA： 26.30000
Density: 1.253g/cm³
LogP: 2.14050

35304-87-1 Relevant articles

Ring-Closing Metathesis Reactions of Acyloxysulfones: Synthesis of γ-Alkylidene Butenolides

Phan, Iris T.,Gilbert, Garrett J.,O'Neil, Gregory W.

supporting information, p. 1867 - 1871 (2015/08/06)

An acyloxysulfone ring-closing metathesi...

A Novel Access to γ-Alkylidenebutenolides: Sequential Stille Couplings of Dibromomethylenebutenolides

Sorg, Achim,Siegel, Konrad,Bru?ckner, Reinhard

, p. 321 - 325 (2007/10/03)

γ-(Dibromomethylene)butenolide (2) and β...

THE SERIES OF SUBSTITUTED BUTANOLIDES AND BUTENOLIDES. IV. 4-ARYLIDENE(HETEROARYLIDENE)-2-BUTENOLIDES

Sorotskaya, L.N.,Badovskaya, L.A.,Kaklyugina, T.Ya.,Belenkii, L.A.,Ignatenko, A.V.,et al.

, p. 159 - 165 (2007/10/02)

A larger number of 4-arylidene- and 4-he...

Cyclisation of Acetylenecarboxylic Acid. Synthesis of γ-Methylenebutyrolactones

Yamamato, Makoto

, p. 582 - 587 (2007/10/02)

Various γ-exo-methylenebutyrolactones ha...

35304-87-1 Process route

: 5-(phenyl(phenylsulfonyl)methyl)furan-2(5H)-one

: 35304-86-0
(Z)-5-phenyl-2,4-pentadien-4-olide

: 35304-87-1
(E)-4-benzylidene-2-butenolide

Conditions

Conditions	Yield
With triethylamine; In dichloromethane; at 0 - 20 ℃; for 15h; Overall yield = 98 %; Overall yield = 19 mg; Inert atmosphere;	71.429 % de

: 676556-25-5
(Z)-5-(1-bromo-1-phenylmethylene)-2(5H)-furanone

: 35304-86-0
(Z)-5-phenyl-2,4-pentadien-4-olide

: 35304-87-1
(E)-4-benzylidene-2-butenolide

Conditions

Conditions	Yield
With acetic acid; zinc; In tetrahydrofuran; at 20 ℃; for 1h; sonication;

35304-87-1 Upstream products

16900-64-4
4-phenylbut-1-en-3-yne-1,1-dicarboxylic acid
497-23-4
2-buten-4-olide
100-52-7
benzaldehyde
676556-25-5
(Z)-5-(1-bromo-1-phenylmethylene)-2(5H)-furanone

Online Inquiry

^*Product Name

CAS

Purity

Quantity



Company name

^*Email

^*Other Description

^*Code

Fields with^*are required

Submit

Pharmaceutical

Agrochemicals

Organic Chemicals

Plant Extract

Others

Home

About Us

Product