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Bicyclo[2.2.2]octane-1,4-diol is a bicyclic organic compound with the molecular formula C8H14O2. It features two fused cyclobutane rings and contains two hydroxyl (OH) groups attached to the carbon atoms at positions 1 and 4 on the bicyclic structure.

1194-44-1

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1194-44-1 Usage

Uses

Used in Organic Synthesis:
Bicyclo[2.2.2]octane-1,4-diol is used as a building block in organic synthesis for the creation of more complex organic compounds. Its unique bicyclic structure and hydroxyl groups make it a valuable intermediate in the synthesis of various organic molecules.
Used in Chemical Research:
Bicyclo[2.2.2]octane-1,4-diol is utilized in chemical research to study the properties and reactions of bicyclic compounds. Its reactivity and structural features provide insights into the behavior of similar compounds and contribute to the advancement of organic chemistry.
Used in Pharmaceutical Industry:
Bicyclo[2.2.2]octane-1,4-diol has potential applications in the pharmaceutical industry as a starting material for the development of new drugs. Its chemical properties and structural characteristics can be exploited to design and synthesize bioactive molecules with therapeutic potential.
Used in Specialty Chemicals Production:
Bicyclo[2.2.2]octane-1,4-diol serves as a starting material for the production of specialty chemicals. Its unique structure and functional groups can be used to create high-value chemicals for various applications, such as coatings, adhesives, and polymers.

Check Digit Verification of cas no

The CAS Registry Mumber 1194-44-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1194-44:
(6*1)+(5*1)+(4*9)+(3*4)+(2*4)+(1*4)=71
71 % 10 = 1
So 1194-44-1 is a valid CAS Registry Number.

1194-44-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name bicyclo[2.2.2]octane-1,4-diol

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1194-44-1 SDS

1194-44-1Relevant academic research and scientific papers

PROCESS FOR PREPARING BICYCLO[2.2.2]OCTANE-1,4-DIOL

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Paragraph 00020, (2021/05/15)

Provided is a process for preparing bicyclo[2.2.2]octane-1,4-diol starting from cyclohexane-1,4-dione. The diene is reacted with certain trialkylsilyl halides or trimethylsilyl trifluormethanesulfonate in the presence of a non-nucleophilic base to afford a silyl-substituted diene, which is in turn reacted with ethylene and subsequently reduced to provide the title compound.

SYNTHESIS OF BICYCLO[2.2.2]OCTANE DERIVATIVES

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Paragraph 0085, (2019/05/02)

Provided is a process for the preparation of certain 1,4-bicyclo[2.2.2]octane derivatives. The new synthetic procedure involves treating 1,4-dimethylene cyclohexane with an oxidizing agent in the presence of a transition metal catalyst to afford an oxo-substituted bicyclo[2.2.2]octane species. This intermediate structure can then be further derivatized. The processes of this disclosure thus affords a novel and simplified means for the commercial production of a wide variety of bicyclo[2.2.2]octane derivatives.

SYNTHESIS OF BICYCLO(2.2.2)OCTANES

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Paragraph 0057, (2018/05/15)

Provided is a process for the preparation of certain 1,4- bicyclo[2.2.2]octane derivatives. The new synthetic procedure involves treating 1,4-dimethylene cyclohexane with an oxidizing agent in the presence of a transition metal catalyst comprising a palla

SYNTHESIS OF 1,4-DISUBSTITUTED BICYCLOOCTANES BY THE DIELS-ALDER REACTION

Geivandov, R.Kh.,Kovshev, E.I.

, p. 461 - 470 (2007/10/02)

Methods were developed for the synthesis of 1,4-diethoxy-, 1,4-dicyano-, and 1,4-diphenyl-1,3-cyclohexadienes.Their adducts with maleic anhydride, acrylonitrile, acrolein, nitroethylene, fumaronitrile, and α-acetoacrylonitrile were converted into the corresponding substituted bicyclooctanes.The configuration of the diene synthesis products was studied by IR and PMR spectroscopy.

SYNTHESIS OF BRIDGEHEAD BICYCLOOCTANOLS

Kopecky, Jan,Smejkal, Jaroslav,Hanus, Vladimir

, p. 1370 - 1375 (2007/10/02)

The paper describes syntheses of bicyclooctan-1-ol, its 4-methyl and 4-phenyl derivatives, and bicyclooctane-1,4-diol.

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