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93232-29-2

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93232-29-2 Usage

General Description

Ethanone, 1,1'-([1,1':2',1''-terphenyl]-4,4''-diyl)bis- is a chemical compound with the molecular formula C30H22O. It is a bis-phenyl compound with a ketone functional group. Ethanone, 1,1'-([1,1':2',1''-terphenyl]-4,4''-diyl)bis- is a yellowish crystalline solid that is primarily used in the field of organic synthesis and materials science. Its unique molecular structure makes it a valuable component in the development of new materials and as a building block in the synthesis of various organic compounds. Additionally, it has potential applications in the field of pharmaceuticals, as well as in the production of dyes and pigments.

Check Digit Verification of cas no

The CAS Registry Mumber 93232-29-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,2,3 and 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 93232-29:
(7*9)+(6*3)+(5*2)+(4*3)+(3*2)+(2*2)+(1*9)=122
122 % 10 = 2
So 93232-29-2 is a valid CAS Registry Number.

93232-29-2SDS

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 1-[4-[2-(4-acetylphenyl)phenyl]phenyl]ethanone

1.2 Other means of identification

Product number -
Other names 4,4''-Diacetyl-o-terphenyl

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:93232-29-2 SDS

93232-29-2Downstream Products

93232-29-2Relevant articles and documents

A New Tetradentate β-Diketonate-Europium Chelate That Can Be Covalently Bound to Proteins for Time-Resolved Fluoroimmunoassay

Yuan, Jingli,Matsumoto, Kazuko,Kimura, Hiroko

, p. 596 - 601 (1998)

A new chlorosulfonylated tetradentate β-diketone, 4,4′-bis(1″,1″,1″,2″,2″,3″,3″- heptafluoro-4″,6″-hexanedion-6″-y1)chlorosulfo-o-terphenyl (BHHCT), was synthesized as a chelating label for Eu3+. BHHCT can be covalently bound to proteins under mild conditions and forms a strongly fluorescent chelate with Eu3+. Bovine serum albumin (BSA) and streptavidin (SA) were labeled with BHHCH-Eu3+, and the latter was used for time-resolved fluoroimmunoassay of a-fetoprotein (AFP) in human sera. A remarkably high sensitivity was obtained, with a detection limit of 4.1 × 10-3 pg/mL, which corresponds to an improvement of about 4-5 orders of magnitude, compared to those of all conventional immunoassays including fluoroimmunoassay, enzyme immunoassay, and radioimmunoassay. The high sensitivity has been attained both by strong fluorescence of the present label and by the extremely suppressed background level brought about by the direct labeling of proteins with the β-diketone-Eu3+ complex. A general consideration and ideas are given for designing ideal label ligands for strongly fluorescent Eu3+ complexes.

A novel biocompatible europium ligand for sensitive time-gated immunodetection

Sayyadi, Nima,Connally, Russell E.,Try, Andrew

supporting information, p. 1154 - 1157 (2016/01/15)

We describe the synthesis of a novel hydrophilic derivative of a tetradentate β-diketone europium ligand that was used to prepare an immunoconjugate probe against Giardia lamblia cysts. We used a Gated Autosynchronous Luminescence Detector (GALD) to obtain high quality delayed luminescence images of cells 30-fold faster than ever previously reported.

Assay of substance in biological sample using labeled probe

-

Referential example 1, (2008/06/13)

A method for analyzing an objective substance, comprsing reacting a labeled probe with an objective substance on a biological sample, said probe comprsing a label substance of the formula (I): wherein A1is an aromatic group, R1is a hydrogen or —COCH2COCnF2n+1and n is an integer of 1-6, which is bonded to a probe selected from the group consisting of nucleic acid, nudeic acid binding potein, low molecular ligand and receptor for ligand (except antibody) to give a fluorescent complex, reacting the complex with an objective substance on a biolgical sample and assaying fluorescence of the resultant fluorescent complex, a labeled nucleic acid probe and a labeled nucleotide. According to the method of the present invention, defects such as hindrance of fluorescence due to contaminant substance, low sensitivity and the like can be resolved, thereby enabling analysis on a tissue.

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