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4-Benzhydrylbenzoic acid is a chemical compound with the molecular formula C20H16O2. It is a white crystalline solid that belongs to the class of benzoic acids, characterized by the presence of a benzhydryl group (a diphenylmethyl group) attached to the 4-position of the benzoic acid backbone. 4-benzhydrylbenzoic acid is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds, as well as its use as an intermediate in the production of various chemical products. Due to its complex structure, 4-benzhydrylbenzoic acid is often synthesized through multi-step processes, highlighting its significance in organic chemistry and the pharmaceutical industry.

6328-81-0

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6328-81-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6328-81-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6328-81:
(6*6)+(5*3)+(4*2)+(3*8)+(2*8)+(1*1)=100
100 % 10 = 0
So 6328-81-0 is a valid CAS Registry Number.
InChI:InChI=1/C20H16O2/c21-20(22)18-13-11-17(12-14-18)19(15-7-3-1-4-8-15)16-9-5-2-6-10-16/h1-14,19H,(H,21,22)

6328-81-0SDS

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 4-benzhydrylbenzoic acid

1.2 Other means of identification

Product number -
Other names 4-Benzhydryl-benzoesaeure

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:6328-81-0 SDS

6328-81-0Relevant academic research and scientific papers

Deoxygenation of tertiary and secondary alcohols with sodium borohydride, trimethylsilyl chloride, and potassium iodide in acetonitrile

Kato, Yuichi,Inoue, Tomoka,Furuyama, Yuuki,Ohgane, Kenji,Sadaie, Mahito,Kuramochi, Kouji

supporting information, (2021/11/16)

The deoxygenation of tertiary and secondary alcohols to give the corresponding alkanes is conventionally performed using an organosilane and a strong acid. In this study, a deoxygenation method was developed for tertiary and secondary alcohols, using trimethylsilane and trimethylsilyl iodide generated in situ from sodium borohydride and trimethylsilyl chloride, and trimethylsilyl chloride and potassium iodide, respectively. With our method, tertiary and secondary alcohols, which provided stable carbocations, were converted into the corresponding alkanes. This paper also presents the optimization of the reaction conditions, the reaction mechanism, as well as the scope and limitations of the method.

Synthesis of enantiomerically enriched triarylmethanes by enantiospecific suzuki-miyaura cross-coupling reactions

Matthew, Smitha C.,Glasspoole, Ben W.,Eisenberger, Patrick,Crudden, Cathleen M.

supporting information, p. 5828 - 5831 (2014/05/20)

The Suzuki-Miyaura cross-coupling of chiral, enantiomerically enriched dibenzylic boronic esters is described. The reaction proceeds with almost complete retention of stereochemistry, providing access to triarylmethanes, compounds that have high biologica

Discovery of new C3aR ligands. Part 1: Arginine derivatives

Denonne, Frederic,Binet, Sophie,Burton, Maggi,Collart, Philippe,Dipesa, Alan,Ganguly, Tanmoy,Giannaras, Alexander,Kumar, Seema,Lewis, Timothy,Maounis, Florence,Nicolas, Jean-Marie,Mansley, Tamsin,Pasau, Patrick,Preda, Dorin,Stebbins, Karin,Volosov, Alexander,Zou, Dong

, p. 3258 - 3261 (2008/02/08)

The synthesis and in vitro binding of several new arginine-containing C3aR ligands are reported. DMPK properties and functional activities of selected compounds have been evaluated. One compound is shown to be active in an in vivo model of airway inflamma

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