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Pentanedial, 3-phenyl-, also known as 3-phenylglutaraldehyde, is an organic compound with the chemical formula C11H10O2. It is a colorless to pale yellow liquid with a molecular weight of 174.20 g/mol. Pentanedial, 3-phenyl- is characterized by the presence of a phenyl group attached to the third carbon of a pentanedial (glutaraldehyde) chain, which consists of a five-carbon aliphatic chain with two aldehyde groups at the terminal positions. Pentanedial, 3-phenyl-, is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. It is also known for its reactivity in various chemical transformations, such as condensation and oxidation reactions, making it a valuable building block in organic synthesis.

7325-50-0

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7325-50-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7325-50-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,2 and 5 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7325-50:
(6*7)+(5*3)+(4*2)+(3*5)+(2*5)+(1*0)=90
90 % 10 = 0
So 7325-50-0 is a valid CAS Registry Number.

7325-50-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyl-glutaraldehyde

1.2 Other means of identification

Product number -
Other names 3-Phenyl-glutaraldehyd

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:7325-50-0 SDS

7325-50-0Relevant academic research and scientific papers

N-[3-(2-CARBOXYETHYL)PHENYL]PIPERIDIN-1-YLACETAMIDE DERIVATIVES AND USE THEREOF AS ACTIVATORS OF SOLUBLE GUANYLATE CYCLASE

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Paragraph 0626-0627, (2015/06/10)

The present application relates to novel substituted 2-(piperidin-1-yl)acetamide derivatives, to processes for preparation thereof, to the use thereof for treatment and/or prevention of diseases, and to the use thereof for production of medicaments for treatment and/or prevention of diseases, especially for treatment and/or prevention of cardiovascular diseases.

Design, synthesis and structure-activity relationship of novel [3.3.1] bicyclic sulfonamide-pyrazoles as potent γ-secretase inhibitors

Aubele, Danielle L.,Truong, Anh P.,Dressen, Darren B.,Probst, Gary D.,Bowers, Simeon,Mattson, Matthew N.,Semko, Chris M.,Sun, Minghua,Garofalo, Albert W.,Konradi, Andrei W.,Sham, Hing L.,Zmolek, Wes,Wong, Karina,Goldbach, Erich,Quinn, Kevin P.,Sauer, John-Michael,Brigham, Elizabeth F.,Wallace, William,Nguyen, Lan,Bova, Michael P.,Hemphill, Susanna S.,Basi, Guriqbal

, p. 5791 - 5794 (2011/10/19)

The structure-activity relationship (SAR) of a novel, potent and metabolically stable series of sulfonamide-pyrazoles that attenuate β-amyloid peptide synthesis via γ-secretase inhibition is detailed herein. Sulfonamide-pyrazoles that are efficacious in reducing the cortical Aβx-40 levels in FVB mice via a single PO dose, as well as sulfonamide-pyrazoles that exhibit selectivity for inhibition of APP versus Notch processing by γ-secretase, are highlighted.

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