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1,1-BIS(4-HYDROXYPHENYL)PENTANE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17181-62-3

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17181-62-3 Usage

Use

Monomers in the production of polycarbonate plastics

Physical State

Colorless solid

Melting Point

High melting point

Solubility

Insoluble in water, soluble in organic solvents

Synthesis

Friedel-Crafts reaction

Reactants in Synthesis

Phenol and 1,1,1,3,3,3-hexachloro-1,3-bis(trimethylsiloxy)disilane

Industrial Applications

a. Production of plastics
b. Thermal stabilizer
c. UV absorber

Other Uses

a. Production of pharmaceuticals
b. Production of agrochemicals

Check Digit Verification of cas no

The CAS Registry Mumber 17181-62-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,8 and 1 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17181-62:
(7*1)+(6*7)+(5*1)+(4*8)+(3*1)+(2*6)+(1*2)=103
103 % 10 = 3
So 17181-62-3 is a valid CAS Registry Number.

17181-62-3SDS

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 4-[1-(4-hydroxyphenyl)pentyl]phenol

1.2 Other means of identification

Product number -
Other names 4,4'-pentylidene-di-phenol

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:17181-62-3 SDS

17181-62-3Downstream Products

17181-62-3Relevant academic research and scientific papers

Metal cation-exchanged montmorillonite (Mn+-mont)-catalysed aromatic alkylation with aldehydes and ketones

Tateiwa, Jun-Ichi,Hayama, Ei,Nishimura, Takahiro,Uemura, Sakae

, p. 1923 - 1928 (2007/10/03)

The alkylation of aromatic compounds with aldehydes and ketones in the presence of a variety of metal cation-exchanged montmorillonites (Mn+-mont; Mn+ = Zr4+, Al3+, Fe3+, Zn2+, H+, Na+) has been investigated. Al3+- and Zr4+-Monts are revealed to be effective as catalysts, while no reaction takes place with Na+-mont. Al3+-Mont-catalysed alkylation of phenol with several aldehydes produces mainly or almost solely the corresponding gem-bis(hydroxyphenyl)alkanes (bisphenols) in good yields, while that with several ketones affords selectively the corresponding alkylphenols in moderate to good yields. The alkylation always occurs at the carbonyl carbon without any skeletal rearrangement and the kind of products depends much on the steric hindrance of an electrophilic intermediary carbocation. The alkylation of anisole, veratrole and p-cresol proceeds well, while that of toluene, benzene, chlorobenzene and nitrobenzene scarcely occurs.

Salicylic acid derivatives

-

, (2008/06/13)

The heat-sensitive recording material disclosed comprises a colorless or pale colored dyestuff precursor, one or more salicylic acid derivative of the formula (1) or metal salt of the derivative and an aliphatic amide compound having 18?60 carbon atoms in molecular structure, and is excellent in thermal response and preservation stability of white portions and images. STR1 wherein X1 and X2 are a hydrogen atom, a halogen atom, an alkyl group, an alkoxy group, an aralkyl group or an aryl group, Y1 and Y2 are an oxygen atom or a sulfur atom, R1 is a hydrogen atom, an alkyl group, an aralkyl group or an aryl group, and R2 is an alkyl group, an alkenyl group, an aralkyl group or an aryl group.

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