154044-13-0 Usage
General Description
Ethyl 5-(4-hydroxyphenyl)pentanoate is an organic compound with the chemical formula C13H18O3. It is a ester formed by the condensation of ethanol and 5-(4-hydroxyphenyl)pentanoic acid. ethyl 5-(4-hydroxyphenyl)pentanoate is commonly used in the fragrance and flavor industry due to its sweet, fruity odor. It is often found in a variety of products, including perfumes, cosmetics, and food flavorings. Additionally, ethyl 5-(4-hydroxyphenyl)pentanoate has been studied for its potential pharmacological properties, such as anti-inflammatory and antioxidant effects.
Check Digit Verification of cas no
The CAS Registry Mumber 154044-13-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,0,4 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 154044-13:
(8*1)+(7*5)+(6*4)+(5*0)+(4*4)+(3*4)+(2*1)+(1*3)=100
100 % 10 = 0
So 154044-13-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H18O3/c1-2-16-13(15)6-4-3-5-11-7-9-12(14)10-8-11/h7-10,14H,2-6H2,1H3
154044-13-0Relevant articles and documents
Structural determinants of 4-chloro-m-cresol required for activation of ryanodine receptor type 1
Jacobson, Alan R.,Moe, Scott T.,Allen,Fessenden, James D.
, p. 259 - 266 (2006)
4-Chloro-m-cresol (4-CmC) is a clinically relevant activator of the intracellular Ca2+ release channel, the ryanodine receptor isoform 1 (RyR1). In this study, the chemical moieties on the 4-CmC molecule required for its activation of RyR1 were
Racemic total synthesis of dactyloidin and demethyldactyloidin through the dl-proline-catalyzed Knoevenagel condensation/[4 + 2] cycloaddition cascade
Tan, Haibo,Liu, Hongxin,Chen, Xinzheng,Chen, Huiyu,Qiu, Shengxiang
, p. 9977 - 9983 (2015/10/12)
An efficient approach towards the first racemic total synthesis of dactyloidin (2) and demethyldactyloidin (3) is described. Their oxygen-bridged tricyclic ketal systems were rapidly constructed by using a remarkable biomimetic Knoevenagel condensation/[4 + 2] cycloaddition cascade as the critical strategy and the 1,5-dicarbonyl segment was assembled by Grignard addition.