1H-Inden-6-ol, 3-(4-hydroxyphenyl)-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.
125791-23-3
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Basic information
- Product Name: 1H-Inden-6-ol, 3-(4-hydroxyphenyl)-2-phenyl-
- Synonyms:
- CAS NO:125791-23-3
- Molecular Formula: C21H16O2
- Molecular Weight: 300.357
- EINECS: N/A
- Product Categories: N/A
- Mol File: 125791-23-3.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: N/A
- Flash Point: N/A
- Appearance: N/A
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: N/A
- Solubility: N/A
- CAS DataBase Reference: 1H-Inden-6-ol, 3-(4-hydroxyphenyl)-2-phenyl-(CAS DataBase Reference)
- NIST Chemistry Reference: 1H-Inden-6-ol, 3-(4-hydroxyphenyl)-2-phenyl-(125791-23-3)
- EPA Substance Registry System: 1H-Inden-6-ol, 3-(4-hydroxyphenyl)-2-phenyl-(125791-23-3)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: N/A
- WGK Germany:
- RTECS:
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 125791-23-3(Hazardous Substances Data)
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125791-23-3 Usage
Derivative of indene
Indene base structure This chemical compound is derived from the indene core structure, which is a fused ring system consisting of a six-membered benzene ring and a five-membered cyclopentadiene ring.Hydroxyl group
-OH The presence of a hydroxyl group (-OH) in the compound contributes to its polarity and allows for the formation of hydrogen bonds, which can affect its solubility, reactivity, and interactions with other molecules.Phenyl group
C6H5A phenyl group (C6H5-) is a stable, planar, and aromatic group consisting of a six-membered ring with alternating single and double carbon-carbon bonds. It is a fundamental structural unit in many organic compounds.4-Hydroxyphenyl group
p-OH on a phenyl ring The 4-hydroxyphenyl group is a phenyl ring (C6H5) with a hydroxyl group (-OH) attached to the carbon at the 4-position (relative to the ring's substitution pattern). This group imparts additional polarity and reactivity to the compound.Unique structure
Complex molecular architecture The combination of indene, phenyl, and hydroxyphenyl groups results in a complex and unique molecular structure that influences its chemical properties and potential applications.Chemical reactivity
Synthesis of organic and pharmaceutical compounds The presence of multiple reactive groups in the molecule allows it to participate in various chemical reactions, making it a valuable building block in the synthesis of other organic and pharmaceutical compounds.Potential applications
Medicine, materials science, and organic chemistry Due to its unique structure and reactivity, 1H-Inden-6-ol, 3-(4-hydroxyphenyl)-2-phenylmay have potential applications in various fields, such as the development of new drugs, advanced materials, or as a synthetic intermediate in organic chemistry.Check Digit Verification of cas no
The CAS Registry Mumber 125791-23-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,7,9 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.Calculate Digit Verification of CAS Registry Number 125791-23:
(8*1)+(7*2)+(6*5)+(5*7)+(4*9)+(3*1)+(2*2)+(1*3)=133
133 % 10 = 3
So 125791-23-3 is a valid CAS Registry Number.
125791-23-3Upstream product
125791-23-3Downstream Products
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1H-Inden-6-ol, 3-(4-hydroxyphenyl)-2-phenyl-
