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2167-55-7

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2167-55-7 Usage

General Description

Bis(4-propan-2-ylphenyl) carbonate is a chemical compound with the molecular formula C23H26O3. It is a carbonate ester and is often used as a reactive plasticizer in the production of polycarbonate resins and other polymers. bis(4-propan-2-ylphenyl) carbonate is known for its high thermal stability, which makes it suitable for use in various applications, including in the production of automotive parts, electrical components, and optical lenses. Bis(4-propan-2-ylphenyl) carbonate is flammable and may release toxic fumes when heated, so it should be handled with care and in accordance with proper safety measures.

Check Digit Verification of cas no

The CAS Registry Mumber 2167-55-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,6 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2167-55:
(6*2)+(5*1)+(4*6)+(3*7)+(2*5)+(1*5)=77
77 % 10 = 7
So 2167-55-7 is a valid CAS Registry Number.
InChI:InChI=1/C19H22O3/c1-13(2)15-5-9-17(10-6-15)21-19(20)22-18-11-7-16(8-12-18)14(3)4/h5-14H,1-4H3

2167-55-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name bis(4-propan-2-ylphenyl) carbonate

1.2 Other means of identification

Product number -
Other names -

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:2167-55-7 SDS

2167-55-7Upstream product

2167-55-7Downstream Products

2167-55-7Relevant articles and documents

Process for the autoxidation of an isopropylphenyl ester

-

, (2008/06/13)

Isopropylphenyl esters are converted to di- or trihydric phenols via a novel autoxidation of the esters at high conversion rates to the corresponding hydroperoxyisopropylphenyl esters in the presence of a catalyst combination comprising at least two members selected from the group consisting of (i) a metal phthalocyanine; (ii) a di-tertiary alkyl peroxide; and (iii) a tertiary alkyl hydroperoxide. Rearrangement of the hydroperoxyisopropylphenyl esters to the corresponding hydroxyphenyl esters and the hydrolysis of the latter compounds provides the phenols in overall yields (from the starting esters) heretofore not obtainable. Novel bis(hydroperoxyisopropylphenyl)carbonates are described which are attractive intermediates for the intermediate bisphenol carbonate or the final hydroquinone hydrolysis product.

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