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1H-Indene-2-carboxylic acid, 6-hydroxy-3-phenyl-, ethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

867187-57-3

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867187-57-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 867187-57-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,7,1,8 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 867187-57:
(8*8)+(7*6)+(6*7)+(5*1)+(4*8)+(3*7)+(2*5)+(1*7)=223
223 % 10 = 3
So 867187-57-3 is a valid CAS Registry Number.

867187-57-3Relevant academic research and scientific papers

Indenone derivatives: A novel template for peroxisome proliferator- activated receptor γ (PPARγ) agonists

Ahn, Jin Hee,Shin, Mi Sik,Jung, Sun Ho,Kang, Seung Kyu,Kim, Kwang Rok,Rhee, Sang Dal,Jung, Won Hoon,Yang, Sung Don,Kim, Seung Jun,Woo, Joo Rang,Lee, Jeong Hyung,Cheon, Hyae Gyeong,Kim, Sung Soo

, p. 4781 - 4784 (2007/10/03)

Agonists of peroxisome proliferator-activated receptor γ(PPAR γ) are of interest as a treatment for diabetes, which prompted the identification of a new class of non-TZD PPAR γ agonist. Moreover, compound 14c has displayed the most active agonistic activi

INDENE DERIVATIVES AND PROCESS FOR THE PREPARATION THEREOF

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Page/Page column 37, (2010/02/14)

The inventive indene derivatives of formula (I) are capable of selectively modulating the activities of peroxisome proliferator activated receptors (PPARs), causing no adverse side effects, and thus, they are useful for the treatment and prevention of disorders modulated by PPARs, i.e., metabolic syndromes such as diabetes, obesity, arteriosclerosis, hyperlipidemia, hyperinsulinism and hypertension, inflammatory diseases such as osteoporosis, liver cirrhosis and asthma, and cancer.

INDENE DERIVATIVES AND PROCESS FOR THE PREPARATION THEREOF

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Page/Page column 22-23, (2008/06/13)

The inventive indene derivatives of formula (I) are capable of selectively modulating the activities of peroxisome proliferator activated receptors (PPARs), causing no adverse side effects, and thus, they are useful for the treatment and prevention of dis

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