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9H-Fluoren-9-ol, 9-[4-(1,1-dimethylethyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 79653-82-0 Structure
  • Basic information

    1. Product Name: 9H-Fluoren-9-ol, 9-[4-(1,1-dimethylethyl)phenyl]-
    2. Synonyms:
    3. CAS NO:79653-82-0
    4. Molecular Formula: C23H22O
    5. Molecular Weight: 314.427
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 79653-82-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 9H-Fluoren-9-ol, 9-[4-(1,1-dimethylethyl)phenyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 9H-Fluoren-9-ol, 9-[4-(1,1-dimethylethyl)phenyl]-(79653-82-0)
    11. EPA Substance Registry System: 9H-Fluoren-9-ol, 9-[4-(1,1-dimethylethyl)phenyl]-(79653-82-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 79653-82-0(Hazardous Substances Data)

79653-82-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79653-82-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,6,5 and 3 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 79653-82:
(7*7)+(6*9)+(5*6)+(4*5)+(3*3)+(2*8)+(1*2)=180
180 % 10 = 0
So 79653-82-0 is a valid CAS Registry Number.

79653-82-0SDS

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 9-(4-tert-butylphenyl)fluoren-9-ol

1.2 Other means of identification

Product number -
Other names 9-(4-tert-butylphenyl)-9-fluorenol

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:79653-82-0 SDS

79653-82-0Relevant articles and documents

A Sc(OTf)3 catalyzed dehydrogenative reaction of electron-rich (hetero)aryl nucleophiles with 9-aryl-fluoren-9-ols

Zhou, Chen,Hu, Chen,Hong, Gang,He, Yuchen,Tang, Zhicong,Wang, Limin

, p. 9615 - 9619 (2019)

A highly efficient dehydrogenative reaction of a series of nucleophiles with 9-aryl-fluoren-9-ols has been realized by using only 2 mol% of Sc(OTf)3 as a catalyst. The corresponding indole-containing 9,9-diarylfluorenes were obtained in up to 99% yield as well as other electron-rich (hetero)arene adducts. The protocol exhibits high selectivity, mild reaction conditions and good substrate compatibility (32 examples). This protocol is further highlighted by its applications in the construction of potential electroluminescent materials.

Fluorene-based compounds, preparation method of compounds and organic electroluminescent device

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Paragraph 0034; 0035; 0036; 0037; 0056; 0057; 0058; 0059, (2020/02/14)

The invention relates to fluorene-based compounds, a preparation method of the compounds and an organic electroluminescent device, and belongs to the field of luminescent materials. The fluorene-basedcompounds have a structural formula shown in the specif

COMPOUND, COATING COMPOSITION COMPRISING THE SAME, ORGANIC LIGHT EMITTING DEVICE USING THE SAME AND METHOD OF MANUFACTURING THE SAME

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Paragraph 0320-0322, (2019/06/27)

The present invention relates to a compound, capable of lowering a driving voltage and improving light efficiency and lifespan characteristics of an organic light emitting device, and to a coating composition including the same, an organic light emitting

The construction of H-shaped fluorescent materials based on building blocks consisting of triphenylamine and fluorene

Zhang, Cheng,Zhang, Yu-Jian,Xiang, Wen-Qin,Hu, Bin,Ouyang, Mi,Xu, Yi,Ma, Chun-An

supporting information; experimental part, p. 520 - 521 (2010/09/05)

A class of complicated 9,9-diarylfluorenes as nonplanar building blocks were synthesized and utilized to prepare a novel H-shaped oligofluorene. High glass transition temperatures and excellent solubility of the obtained oligomers indicated the 9,9diarylfluorenes would be promising building blocks for the construction of H-shaped optoelectronic materials.

Versatile and Convenient Lattice Hosts derived from Singly Bridged Triarylmethane Frameworks, X-Ray Crystal Structures of Three Inclusion Compounds

Weber, Edwin,Doerpinghaus, Norbert,Csoeregh, Ingeborg

, p. 2167 - 2177 (2007/10/02)

A new family of host molecules, based on the singly bridged triarylmethanol and triarylacetic acid frameworks, is described.These hosts form crystalline inclusions with a variety of uncharged organic molecules ranging from protic dipolar to apolar compounds (130 different species).The formation and stoicheiometry depend in a systematic manner on structural parameters of the host, such as the nature of the functional group and the substituents, and on the substituent positions.The crystal structures of three inclusion compounds have been studied by X-ray diffraction.They reveal the building principles of the new inclusion family.In the crystals of 1a*benzene (8:3), the benzene is interstitially entrapped by H-bonded tetramer clusters of 1a.Crystals of 1a*dioxane (4:3) are built of H-bonded 2:1 host-guest complexes including interstitial molecules of dioxane.In the case of 4c*EtOH (1:1), the building principle is formation of 2:2 host-guest clusters via a twelve-membered H-bonded ring.

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