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9-Phenoxy-nonanoic acid, also known as 9-phenyl-9-oxanonanoic acid, is an organic compound with the chemical formula C15H18O3. It is a white crystalline solid that is soluble in organic solvents and has a molecular weight of 246.30 g/mol. 9-phenoxy-nonanoic acid is characterized by a phenyl group attached to a nine-carbon alkyl chain, which terminates in a carboxylic acid group. It is used in various applications, including as an intermediate in the synthesis of pharmaceuticals and agrochemicals, due to its ability to form esters and other derivatives. The compound's properties, such as its lipophilicity and potential for hydrogen bonding, make it a versatile building block in the creation of more complex molecules.

7170-43-6

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7170-43-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7170-43-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,7 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7170-43:
(6*7)+(5*1)+(4*7)+(3*0)+(2*4)+(1*3)=86
86 % 10 = 6
So 7170-43-6 is a valid CAS Registry Number.

7170-43-6Downstream Products

7170-43-6Relevant academic research and scientific papers

4-DIMETHYLAMINOBUTYRIC ACID DERIVATIVES

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Page/Page column 15, (2009/10/31)

This invention relates to novel 4-dimethylaminobutyric acid derivatives of the formula wherein A1, A2, R1, m and n are as defined in the description and in the claims, as well as pharmaceutically acceptable salts thereof. These compounds inhibit carnitine palmitoyl transferase (CPT) activity, in particular CPT2 activity, and can be used as medicaments in methods for the treatment of diseases modulated by CPT2 inhibitors.

Method of inhibiting parasitic activity

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, (2008/06/13)

A method of inhibiting parasitic activity is disclosed in which the biosynthesis, structure and/or function of the glycosyl phosphatidylinositol (GPI) anchor of said parasite may be affected by incorporating into said GPI anchor selected analogs of myristic acid containing various heteroatoms, substituents and unsaturated bonds, including ester-containing analogs, ketocarbonyl-containing analogs, sulfur-containing analogs, double bond- and triple bond-containing analogs, aromatic moiety-containing analogs, nitrated analogs and halogenated analogs.

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