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159424-07-4

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159424-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 159424-07-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,4,2 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 159424-07:
(8*1)+(7*5)+(6*9)+(5*4)+(4*2)+(3*4)+(2*0)+(1*7)=144
144 % 10 = 4
So 159424-07-4 is a valid CAS Registry Number.

159424-07-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name [3,5-bis(4-tert-butylbenzoyl)phenyl]-(4-tert-butylphenyl)methanone

1.2 Other means of identification

Product number -
Other names Methanone,1,3,5-benzenetriyltris[[4-(1,1-dimethylethyl)phenyl]

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:159424-07-4 SDS

159424-07-4Relevant articles and documents

Exploratory and Mechanistic Studies of the Trimerization Reaction of Benzoylacetylenes in the Presence of Secondary Amine

Matsuda, Kenji,Nakamura, Nobuo,Iwamura, Hiizu

, p. 1765 - 1768 (1994)

A variety of benzoylacetylenes are trimerized to give the corresponding 1,3,5-tribenzoylbenzenes when heated with a catalytic amount of diethylamine.A large amount of diethylamine gives γ-(diethylamino)propenoylbenzene at the expense of 1,3,5-tribenzoylbe

Design, synthesis, and characterization of three kinds of π-cross-conjugated hexacarbenes with high-spin (S = 6) ground states

Matsuda, Kenji,Nakamura, Nobuo,Takahashi, Kazuyuki,Inoue, Katsuya,Koga, Noboru,Iwamura, Hiizu

, p. 5550 - 5560 (2007/10/02)

Three kinds of nonlinearly π-conjugated hexadiazo compounds were obtained from the corresponding hexaketones for which cyclotrimerizaton of the ethynyl ketones to form 1,3,5-triaroylbenzenes and deoxygenation of a calix[6]arene were key steps. The diazo c

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