What is the Bicyclo[2.2.1]heptane-2,3-dimethanol?

Bicyclo[2.2.1]heptane-2,3-dimethanol is , while it's Molecular Formula is C9H16O2. Given the scarcity of detailed information on the specific uses of Bicyclo[2.2.1]heptane-2,3-dimethanol, the following applications are inferred based on its chemical structure and classification: Used in Research and Development: Bicyclo[2.2.1]heptane-2,3-dimethanol is used as a chemical intermediate for the synthesis of more complex organic compounds in research and development settings. Its unique bicycloheptane ring and hydroxy functional groups make it a valuable building block for creating novel molecules with potential applications in various fields. Used in Specialty Chemicals Industry: In the specialty chemicals industry, Bicyclo[2.2.1]heptane-2,3-dimethanol may serve as a key component in the production of specific chemical products. Its presence in this industry could be attributed to its structural features, which might offer unique reactivity or stability in the synthesis of certain compounds. Used in Pharmaceutical Development: Although not explicitly mentioned, the compound's classification as a bicyclic monoterpenoid suggests potential use in the pharmaceutical industry. Bicyclo[2.2.1]heptane-2,3-dimethanol could be employed as a precursor in the development of new drugs, leveraging its structural properties to target specific biological pathways or mechanisms.

What is the CAS number for Bicyclo[2.2.1]heptane-2,3-dimethanol?

The CAS number of Bicyclo[2.2.1]heptane-2,3-dimethanol is 45849-05-6.

What is Bicyclo[2.2.1]heptane-2,3-dimethanol (45849-05-6) used for?

Bicyclo[2.2.1]heptane-2,3-dimethanol is an organic chemical compound characterized by its molecular formula C9H16O2. It features a unique bicycloheptane ring structure adorned with two hydroxy functional groups. Bicyclo[2.2.1]heptane-2,3-dimethanol is classified under the bicyclic monoterpenoids, a subset of monoterpenoids that include a cyclopropane ring within their structure. Primarily, it falls under the category of Bicyclo[2.2.1]heptanes and their derivatives. Given the limited information on its applications, toxicity, and physical properties, Bicyclo[2.2.1]heptane-2,3-dimethanol is likely utilized in research settings or within specialized industrial applications.InChI:InChI=1/C9H16O2/c10-4-8-6-1-2-7(3-6)9(8)5-11/h6-11H,1-5H2

What is the Bicyclo[2.2.1]heptane-2,3-dimethanol?

Bicyclo[2.2.1]heptane-2,3-dimethanol is , while it's Molecular Formula is C9H16O2. Given the scarcity of detailed information on the specific uses of Bicyclo[2.2.1]heptane-2,3-dimethanol, the following applications are inferred based on its chemical structure and classification: Used in Research and Development: Bicyclo[2.2.1]heptane-2,3-dimethanol is used as a chemical intermediate for the synthesis of more complex organic compounds in research and development settings. Its unique bicycloheptane ring and hydroxy functional groups make it a valuable building block for creating novel molecules with potential applications in various fields. Used in Specialty Chemicals Industry: In the specialty chemicals industry, Bicyclo[2.2.1]heptane-2,3-dimethanol may serve as a key component in the production of specific chemical products. Its presence in this industry could be attributed to its structural features, which might offer unique reactivity or stability in the synthesis of certain compounds. Used in Pharmaceutical Development: Although not explicitly mentioned, the compound's classification as a bicyclic monoterpenoid suggests potential use in the pharmaceutical industry. Bicyclo[2.2.1]heptane-2,3-dimethanol could be employed as a precursor in the development of new drugs, leveraging its structural properties to target specific biological pathways or mechanisms.

What is the CAS number for Bicyclo[2.2.1]heptane-2,3-dimethanol?

The CAS number of Bicyclo[2.2.1]heptane-2,3-dimethanol is 45849-05-6.

What is Bicyclo[2.2.1]heptane-2,3-dimethanol (45849-05-6) used for?

Bicyclo[2.2.1]heptane-2,3-dimethanol is an organic chemical compound characterized by its molecular formula C9H16O2. It features a unique bicycloheptane ring structure adorned with two hydroxy functional groups. Bicyclo[2.2.1]heptane-2,3-dimethanol is classified under the bicyclic monoterpenoids, a subset of monoterpenoids that include a cyclopropane ring within their structure. Primarily, it falls under the category of Bicyclo[2.2.1]heptanes and their derivatives. Given the limited information on its applications, toxicity, and physical properties, Bicyclo[2.2.1]heptane-2,3-dimethanol is likely utilized in research settings or within specialized industrial applications.InChI:InChI=1/C9H16O2/c10-4-8-6-1-2-7(3-6)9(8)5-11/h6-11H,1-5H2

Product classification

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45849-05-6

Product Name：Bicyclo[2.2.1]heptane-2,3-dimethanol
Molecular Formula：C₉H₁₆O₂
Purity：99%
Molecular Weight：156.225

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Product Details;

CasNo： 45849-05-6

Molecular Formula： C₉H₁₆O₂

factory and supplier 45849-05-6 Bicyclo[2.2.1]heptane-2,3-dimethanol in stock

Molecular Formula:C9H16O2
Molecular Weight:156.225
Vapor Pressure:0mmHg at 25°C
Refractive Index:1.4982 (589.3 nm 30.5℃)
Boiling Point:306.124°C at 760 mmHg
Flash Point:150.617°C
PSA：40.46000
Density:1.097g/cm³
LogP:0.63330

Bicyclo[2.2.1]heptane-2,3-dimethanol(Cas 45849-05-6) Usage

General Description

Bicyclo[2.2.1]heptane-2,3-dimethanol is an organic chemical compound with the molecular formula C9H16O2. It consists of a bicycloheptane ring structure and two hydroxy functional groups. It belongs to the class of organic compounds known as bicyclic monoterpenoids. These are monoterpenoids with a structure containing two rings, one of which is a cyclopropane ring. The primary classification of this compound is Bicyclo[2.2.1]heptanes and derivatives. As of now, there's not much information available about its usage, toxicity or physical properties, indicating that it may be largely used in research or in specialized industrial processes.

InChI:InChI=1/C9H16O2/c10-4-8-6-1-2-7(3-6)9(8)5-11/h6-11H,1-5H2

45849-05-6 Relevant articles

Development of effective bidentate diphosphine ligands of ruthenium catalysts toward practical hydrogenation of carboxylic acids

Saito, Susumu,Wen, Ke,Yoshioka, Shota

supporting information, p. 1510 - 1524 (2021/06/18)

Hydrogenation of carboxylic acids (CAs) ...

Epimerization of Tertiary Carbon Centers via Reversible Radical Cleavage of Unactivated C(sp3)-H Bonds

Wang, Yaxin,Hu, Xiafei,Morales-Rivera, Cristian A.,Li, Guo-Xing,Huang, Xin,He, Gang,Liu, Peng,Chen, Gong

supporting information, p. 9678 - 9684 (2018/07/21)

Reversible cleavage of C(sp3)-H bonds ca...

Self-immobilizing precatalysts: Norbornene-bridged zirconium ansa-metallocenes

Polo, Eleonora,Forlini, Fabrizio,Bertolasi, Valerio,Boccia, Antonella Caterina,Sacchi, Maria Carmela

experimental part, p. 1544 - 1556 (2009/07/30)

We report here the synthesis of new teth...

Synthesis of and hydroformylation with fluoro-substituted bidentate phosphine ligands

-

, (2008/06/13)

Hydroformylation of alkenes to aldehydes...

45849-05-6 Process route

: 821-11-4
trans-butene-1,4-diol

: 542-92-7,25568-84-7,7313-32-8
cyclopenta-1,3-diene

: 45849-05-6
2,3-bis(hydroxymethyl) bicyclo [2,2,1] heptane

Conditions

Conditions	Yield
With Hg; Pd on charcoal; In ethanol;

: 6004-79-1
(exo)-Hexahydro-4,7-methanoisobenzofuran-1,3-dione

: 45849-05-6
2,3-bis(hydroxymethyl) bicyclo [2,2,1] heptane