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Benzoic acid, 3,5-bis[5-[4-(1,1-dimethylethyl)phenyl]-1,3,4-oxadiazol-2-yl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

175791-98-7

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175791-98-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 175791-98-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,5,7,9 and 1 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 175791-98:
(8*1)+(7*7)+(6*5)+(5*7)+(4*9)+(3*1)+(2*9)+(1*8)=187
187 % 10 = 7
So 175791-98-7 is a valid CAS Registry Number.

175791-98-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-bis<5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl>benzoic acid

1.2 Other means of identification

Product number -
Other names 3,5-Bis-[5-(4-tert-butyl-phenyl)-[1,3,4]oxadiazol-2-yl]-benzoic acid

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:175791-98-7 SDS

175791-98-7Relevant academic research and scientific papers

Synthesis and self-association of first-generation 1,3,4-oxadiazole-containing dendrimers

Kraft, Arno

, p. 1463 - 1471 (1997)

Two 1,3,4-oxadiazole-containing dendrimers, 14 and 15, have been prepared employing a palladium-catalyzed carbonylation reaction as the key step of the synthesis. In order to shorten the reaction sequence, a new oxadiazole synthesis has been developed bas

Self-association of branched and dendritic aromatic amides

Kraft, Arno,Osterod, Frank

, p. 1019 - 1025 (2007/10/03)

Several branched and dendritic aromatic amides have been obtained by reacting tris(4-aminophenyl)-methane 3 either with aryl iodide 1 in a Pd-catalysed carbonylation or with carboxylic acids in the presence of the coupling agent triphenyl phosphite. Nonpolar aromatic substituents and solubilising groups at the periphery ensured that the resulting oligoamides were soluble in chloroform, whereas amide groups in the structural centre of the molecules accounted for strong self-association through hydrogen bonding in solution as evidenced by 1H NMR and vapour-pressure osmometry data. An alternative approach towards branched aramides is also presented which was based on the self-assembly of 1,3,5-tris(4,5-dihydroimidazol-2-yl)benzene 12 and various (amido)carboxylic acids.

Self-association of poly(aramide) dendrimers

Osterod, Frank,Kraft, Arno

, p. 1435 - 1436 (2007/10/03)

Two poly(aramide) dendrimers, which possess electron-deficient 1,3,4-oxadiazole and aromatic systems linked by amide units to a triphenylmethane core, strongly self-associate in chloroform solution through hydrogen bonding.

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