90199-12-5 Usage
Type of compound
Diol
Explanation
A diol is a type of alcohol that contains two hydroxyl groups (-OH) attached to a carbon chain or ring.
Explanation
The cyclohexane ring is a common structural feature in many organic compounds, providing a stable and rigid framework for the attachment of functional groups.
Explanation
The presence of two hydroxyl groups in the compound gives it the characteristic properties of a diol, such as increased polarity and hydrogen bonding.
Explanation
The ethynyl group is a linear functional group containing a carbon-carbon triple bond, which contributes to the compound's reactivity and potential applications.
Explanation
Due to its unique structure and functional groups, 1,4-Cyclohexanediol, 1-ethynyl(7CI) can be used as a building block or intermediate in the synthesis of various organic compounds, including pharmaceuticals, polymers, and other industrial products.
Explanation
The compound's unique properties and potential applications make it an attractive target for further research and development in the fields of organic chemistry, materials science, and pharmaceutical chemistry.
Cyclohexane ring
Six carbon atoms arranged in a closed ring structure
Hydroxyl groups
Two -OH groups attached to the cyclohexane ring
Ethynyl group
A carbon-carbon triple bond (-C≡CH)
Applications
Organic synthesis, pharmaceuticals, polymers, and industrial products
Research interest
Subject of interest for researchers and industrial chemists
Check Digit Verification of cas no
The CAS Registry Mumber 90199-12-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,1,9 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 90199-12:
(7*9)+(6*0)+(5*1)+(4*9)+(3*9)+(2*1)+(1*2)=135
135 % 10 = 5
So 90199-12-5 is a valid CAS Registry Number.
90199-12-5Relevant academic research and scientific papers
Preparation method of axially chiral methylene cyclohexane derivative
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Paragraph 0030; 0032, (2021/07/01)
The invention discloses a preparation method of an axially chiral methylene cyclohexane derivative. The preparation method comprises the following step of: performing an enantioselective hydrosilylation addition reaction on an exoallene compound serving as a raw material under the action of a copper catalyst, a ligand and silane to obtain the axially chiral methylene cyclohexane derivative. According to the invention, the one-step method is adopted, a system is simple, operation is convenient and fast, the axially chiral methylene cyclohexane derivative can be obtained through treatment without secondary conversion, the method is adapted to a wide range of substrates and resistant to various substrates and silane, and the product yield and the enantiomeric excess value of the method are not inferior to the product yield and the enantiomeric excess value of a traditional method. The invention provides a new synthesis means for developing a class of axially chiral methylene cyclohexane derivatives, and the method has economic practicability and industrial application prospects.
