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7-phenoxy-heptanoic acid is an organic compound with the chemical formula C13H16O3. It is a derivative of heptanoic acid, featuring a phenoxy group attached to the seventh carbon atom. 7-phenoxy-heptanoic acid is characterized by its molecular structure, which includes a seven-carbon chain with a carboxyl group at one end and a phenoxy group at the other. It is a white crystalline solid and is soluble in organic solvents. 7-phenoxy-heptanoic acid has potential applications in the pharmaceutical and chemical industries, particularly as an intermediate in the synthesis of various drugs and other organic compounds. Its properties, such as its reactivity and solubility, make it a valuable building block for the creation of more complex molecules.

7170-42-5

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7170-42-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7170-42-5 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 7170-42:
(6*7)+(5*1)+(4*7)+(3*0)+(2*4)+(1*2)=85
85 % 10 = 5
So 7170-42-5 is a valid CAS Registry Number.

7170-42-5Relevant academic research and scientific papers

2-AMINO-1,3,4-THIADIAZINE AND 2-AMINO-1,3,4-OXADIAZINE BASED ANTIFUNGAL AGENTS

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Page/Page column 78, (2017/02/09)

The invention provides a compound which is a diazine of formula (I) or a tautomer thereof, or a pharmaceutically acceptable salt thereof, for use as an antifungal agent: (I) wherein X, N', C', A and E are as defined herein. The invention also provides a compound of Formula (I) as defined herein.

Liquid Crystalline Properties of Cholesteryl ω-Arylalkanoates

Koden, Mitsuhiro,Miyake, Shiro,Takenaka, Shunsuke,Kusabayashi, Shigekazu

, p. 2387 - 2390 (2007/10/02)

The thermal properties of the homologous series of cholesteryl ω-(4-benzoylphenyl)- (I), ω-(4-benzylphenyl)- (II), ω-benzoyl- (III), and ω-phenoxyalkanoate (IV) have been investigated.For series I and II the cholesteric-isotropic (Ch-I) transition temperatures, enthalpies, and entropies show a remarkable alternation.For series III and IV, the transition temperatures, enthalpies, and entropies exhibit weak alternation and their trends are opposite to those for series I and II, and the cholesteryl ω-phenylalkanoates.The cholesteric-isotropic transition temperatures are discussed in terms of the geometrical and electrical alternations stemming from the terminal aryl groups, and also the relative importance between these two terms.

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