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14160-38-4

14160-38-4

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14160-38-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14160-38-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,1,6 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 14160-38:
(7*1)+(6*4)+(5*1)+(4*6)+(3*0)+(2*3)+(1*8)=74
74 % 10 = 4
So 14160-38-4 is a valid CAS Registry Number.

14160-38-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-tert-butyl-6-(5-tert-butyl-3,6-dioxocyclohexa-1,4-dien-1-yl)cyclohexa-2,5-diene-1,4-dione

1.2 Other means of identification

Product number -
Other names 3,3'-di-t-butylbiphenyl-2,5,2',5'-diquinone

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:14160-38-4 SDS

14160-38-4Relevant articles and documents

Influence of the position of tert-butyl substituents on reactivity of quinone dimers yielding dibenzofuran-1,4-diones

Hayashi, Naoto,Kanda, Akifumi,Higuchi, Hiroyuki,Ninomiya, Keiko

experimental part, p. 1361 - 1367 (2009/07/05)

Reactivity of two isomeric quinone dimers, 5,5'-di-tert-butyl-2,2'-bisbenzoquinone (2) and 6,6'-di-tert-butyl-2,2'-bisbenzoquinone (3) have been compared. Both quinone dimers underwent thermal cyclization in ethanol to give dibenzofuran-1,4-diones exclusi

OXIDATIVE COUPLING REACTION OF 2-HALOPHENOLS WITH K3Fe(CN)6 IN BENZENE SOLUTION

Tashiro, Masashi,Yoshiya, Haruo

, p. 653 - 660 (2007/10/02)

The oxidative coupling of twelve 2-halophenols (1a-1l) was carried out with K3Fe(CN)6 in benzene solution to obtain the corresponding dibenzofuran derivatives.However, only a small amount of the desired dibenzofurans such as 2,6-di-tert-butyl-8-methoxybenzofuran-1,4-quinone (9) and 4,8-di-tert-butyl-2,6-di-isopropyl-1-hydroxydibenzofuran (11) were obtained from 2-bromo-6-tert-butyl-4-methoxy- (1d) and 2-bromo-4-tert-butyl-6-isopropylphenol (1g), respectively.In the other cases, alternative type of products or tarry materials were formed.

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