What is the Bicyclo[2.2.2]octan-2-one?

Bicyclo[2.2.2]octan-2-one is , while it's Molecular Formula is C8H12 O. Used in Pharmaceutical Industry: Bicyclo[2.2.2]octan-2-one is used as a building block for the synthesis of various pharmaceuticals. Its unique structure and reactivity allow for the development of new drug candidates with potential therapeutic benefits. Used in Agrochemical Industry: In the agrochemical sector, Bicyclo[2.2.2]octan-2-one serves as a key intermediate in the production of various agrochemicals. Its ability to be modified and functionalized contributes to the creation of effective compounds for crop protection and pest control. Used in Fragrance Industry: Bicyclo[2.2.2]octan-2-one is utilized as a precursor in the synthesis of fragrance ingredients. Its unique molecular structure enables the development of novel scents and aromas for use in perfumes, cosmetics, and other fragrance applications. Used in Organic Chemistry Research: As a versatile compound with a strained ring system, Bicyclo[2.2.2]octan-2-one is employed in organic chemistry research to explore new reaction pathways, develop innovative synthetic methods, and study the effects of ring strain on chemical reactivity and selectivity.

What is the CAS number for Bicyclo[2.2.2]octan-2-one?

The CAS number of Bicyclo[2.2.2]octan-2-one is 2716-23-6.

What is Bicyclo[2.2.2]octan-2-one (2716-23-6) used for?

Bicyclo[2.2.2]octan-2-one is a bicyclic ketone compound characterized by its unique three-dimensional structure. It features a rigid and strained ring system that endows it with distinctive reactivity and stereochemistry, making it a valuable precursor in the field of organic chemistry. Bicyclo[2.2.2]octan-2-one is versatile and can be functionalized or modified to create a wide range of molecular structures with diverse properties and applications.InChI:InChI=1/C8H12O/c9-8-5-6-1-3-7(8)4-2-6/h6-7H,1-5H2

What is the Bicyclo[2.2.2]octan-2-one?

Bicyclo[2.2.2]octan-2-one is , while it's Molecular Formula is C8H12 O. Used in Pharmaceutical Industry: Bicyclo[2.2.2]octan-2-one is used as a building block for the synthesis of various pharmaceuticals. Its unique structure and reactivity allow for the development of new drug candidates with potential therapeutic benefits. Used in Agrochemical Industry: In the agrochemical sector, Bicyclo[2.2.2]octan-2-one serves as a key intermediate in the production of various agrochemicals. Its ability to be modified and functionalized contributes to the creation of effective compounds for crop protection and pest control. Used in Fragrance Industry: Bicyclo[2.2.2]octan-2-one is utilized as a precursor in the synthesis of fragrance ingredients. Its unique molecular structure enables the development of novel scents and aromas for use in perfumes, cosmetics, and other fragrance applications. Used in Organic Chemistry Research: As a versatile compound with a strained ring system, Bicyclo[2.2.2]octan-2-one is employed in organic chemistry research to explore new reaction pathways, develop innovative synthetic methods, and study the effects of ring strain on chemical reactivity and selectivity.

What is the CAS number for Bicyclo[2.2.2]octan-2-one?

The CAS number of Bicyclo[2.2.2]octan-2-one is 2716-23-6.

What is Bicyclo[2.2.2]octan-2-one (2716-23-6) used for?

Bicyclo[2.2.2]octan-2-one is a bicyclic ketone compound characterized by its unique three-dimensional structure. It features a rigid and strained ring system that endows it with distinctive reactivity and stereochemistry, making it a valuable precursor in the field of organic chemistry. Bicyclo[2.2.2]octan-2-one is versatile and can be functionalized or modified to create a wide range of molecular structures with diverse properties and applications.InChI:InChI=1/C8H12O/c9-8-5-6-1-3-7(8)4-2-6/h6-7H,1-5H2

Product classification

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2716-23-6

Product Name:Bicyclo[2.2.2]octan-2-one
Molecular Formula:C8H12 O
Molecular Weight:124.183

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Product Details

pd_meltingpoint:178-179 °C

Purity:99%

Manufacturer supply high quality Bicyclo[2.2.2]octan-2-one 2716-23-6 with ISO standards

Molecular Formula:C8H12 O
Molecular Weight:124.183
Vapor Pressure:0.305mmHg at 25°C
Melting Point:178-179 °C
Boiling Point:201.6°Cat760mmHg
Flash Point:68.7°C
PSA：17.07000
Density:1.039g/cm³
LogP:1.76560

Bicyclo[2.2.2]octan-2-one(Cas 2716-23-6) Usage

General Description

Bicyclo[2.2.2]octan-2-one is a bicyclic ketone compound with a unique three-dimensional structure. It is often used as a building block in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and fragrance ingredients. The compound's rigid and strained ring system confers unique reactivity and stereochemistry, making it a valuable precursor in organic chemistry. Bicyclo[2.2.2]octan-2-one can undergo various chemical reactions to functionalize the carbonyl group or modify the ring structure, allowing for the creation of diverse molecular structures with different properties and applications.

InChI:InChI=1/C8H12O/c9-8-5-6-1-3-7(8)4-2-6/h6-7H,1-5H2

2716-23-6 Relevant articles

OXIDATIVE DESULFONYLATION. PHENYL VINYL SULFONE AS A KETENE SYNTHETIC EQUIVALENT

Little, R. Daniel,Myong, Sun Ok

, p. 3339 - 3342 (1980)

α-Sulfonyl carbanions undergo oxidative ...

-

Walborsky,Loncrini

, p. 6399 (1954)

-

Bly et al.

, p. 2235 (1970)

-

Morrill,K. et al.

, p. 907 - 911 (1977)

NOVEL FUSED BRIDGED BICYCLIC HETEROARYL SUBSTITUTED 6-ALKYLIDENE PENEMS AS POTENT BETA-LACTAMASE INHIBITORS

-

Page/Page column 13; 14, (2011/12/12)

A compound of formula (I) or formula (Ia...

Thermal chemistry of bicyclo[4.2.0]oct-2-enes

Powers, David C.,Leber, Phyllis A.,Gallagher, Sarah S.,Higgs, Andrew T.,McCullough, Lynne A.,Baldwin, John E.

, p. 187 - 194 (2007/10/03)

At 300 °C, bicyclo[4.2.0]oct-2-ene (1) i...

Thermal reactions of 7-d- and 8-d-bicyclo[4.2.0]oct-2-enes

Baldwin, John E.,Leber, Phyllis A.,Powers, David C.

, p. 10020 - 10021 (2007/10/03)

The gas phase thermal reactions exhibite...

Activated cycloheptenone dienophiles. A versatile approach to 6,7-fused ring targets

Liu, Hsing-Jang,Yeh, Wen-Lung,Browne, Eric N. C.

, p. 1135 - 1147 (2007/10/03)

Several 2-carbalkoxy-2-cyclohepten-1-one...

2716-23-6 Process route

: 18684-63-4
bicyclo[2.2.2]octan-2-ol

: 2716-23-6
bicyclo[2.2.2]octan-2-one

Conditions

Conditions	Yield
With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In 1,1-dichloroethane; for 1h; Reflux;	87%
With chromic acid; In acetone;	70%
With cycloheptanone; aluminum isopropoxide; In benzene; at 80 ℃; Thermodynamic data; Mechanism; ΔG_ox and ΔG_r;
With chromium(VI) oxide;
With cycloheptanone; aluminum isopropoxide; In benzene; at 80 ℃;