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Phenol, 2-[9-(4-hydroxyphenyl)-9H-fluoren-9-yl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

152480-63-2

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152480-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 152480-63-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,2,4,8 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 152480-63:
(8*1)+(7*5)+(6*2)+(5*4)+(4*8)+(3*0)+(2*6)+(1*3)=122
122 % 10 = 2
So 152480-63-2 is a valid CAS Registry Number.

152480-63-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[9-(4-hydroxyphenyl)fluoren-9-yl]phenol

1.2 Other means of identification

Product number -
Other names 9-(4-hydroxyphenyl)-9(2-hydroxyphenyl)-fluorene

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:152480-63-2 SDS

152480-63-2Downstream Products

152480-63-2Relevant academic research and scientific papers

Condensation of 9-fluorenone and phenol using an ionic liquid and a mercapto compound synergistic catalyst

Lei, Yan,Yu, Limei,Shen, Maochang,Luo, Shikang,Gao, Zhanxian

supporting information, p. 15700 - 15705 (2019/10/19)

A series of ionic liquids (ILs) were synthesized and their Hammett acidities (H0) were determined using 4-nitroaniline as the indicator. The relationship among IL's structure, the acid strength, and the catalytic performance in the condensation reaction of 9-fluorenone with phenol was discussed. The effective H0 range of ionic liquids that can catalyse the condensation reaction was obtained. Moreover, the catalysis of the mercapto compound co-catalyst was also systematically studied. According to the analysis of how the structure of the sulfydryl co-catalyst affects the percent conversion of 9-fluorenone and the selectivity of BHPF, a mechanism for the reaction in the IL-thiol cooperative catalytic system was proposed. The present work gave a clear clue to design novel IL catalysts for the synthesis of BHPF.

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