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Benzoic acid, 4-[(1-oxohexyl)amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

109506-41-4

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109506-41-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109506-41-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,5,0 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 109506-41:
(8*1)+(7*0)+(6*9)+(5*5)+(4*0)+(3*6)+(2*4)+(1*1)=114
114 % 10 = 4
So 109506-41-4 is a valid CAS Registry Number.

109506-41-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(hexanoylamino)benzoic acid

1.2 Other means of identification

Product number -
Other names Benzoic acid,4-[(1-oxohexyl)amino]

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:109506-41-4 SDS

109506-41-4Relevant academic research and scientific papers

ARAMID AMPHIPHILE SELF-ASSEMBLED NANOSTRUCTURES

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Paragraph 0246, (2020/12/29)

Aramids and nanostructures formed from the aramids are described.

Novel Oxazolidinone-Based Peroxisome Proliferator Activated Receptor Agonists: Molecular Modeling, Synthesis, and Biological Evaluation

Fresno,Macías-González,Torres-Zaguirre,Romero-Cuevas,Sanz-Camacho,Elguero,Pavón,Rodríguez De Fonseca,Goya,Pérez-Fernández

, p. 6639 - 6652 (2015/09/07)

(Figure Presented). A series of new peroxisome proliferator activated receptors (PPARs) chiral ligands have been designed following the accepted three-module structure comprising a polar head, linker, and hydrophobic tail. The majority of the ligands inco

Synthesis and antiaggregator activity of some new derivatives of 4H-benzopyran-4-one

Goeker, H.,Ayhan, G.,Tuncbilek, M.,Ertan, R.,Leoncini, G.,et al.

, p. 561 - 568 (2007/10/02)

A series of 2--4H-1-benzopyran-4-one analogues 7a-7e was synthesized by the reaction with 3',4'-diaminoflavone and aliphatic carboxylic acids. 3',4'-Diaminoflavone 6 was prepared via the reduction of 2-(4-amino-3-nitrophenyl)-4H-1-benzopyran-4-one 5a.The compounds 7a-e and 14a-f were tested in vitro for their inhibitory activities against human platelet aggregation induced by collagen, ADP and A23187.The compound with a COOR group as a side chain, 2-(2-akyloxycarbonyl-2,3-dihydro-1,4-benzodioxin -6-yl)-4H-1-benzopyran-4-one 14a-f, haspotent activity, and so compound 13 was also prepared as an analogue of series 14 and tested for its antiaggregator activity. 4H-1-benzopyran-4-one/ benzodioxane/ benzimidazole/ human platelet/ aggregation

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