10528-64-0 Usage
General Description
4-(4-isopropylphenyl)butan-2-one, also known as p-Isobutylacetophenone, is a chemical compound with a molecular formula of C14H18O. It is a fragrant organic compound commonly used in the production of perfumes and other scented products. It is a colorless to pale yellow liquid with a sweet, floral, and fruity odor. 4-(4-isopropylphenyl)butan-2-one is widely used in the fragrance industry due to its desirable scent properties. Additionally, it is also used in the production of flavoring agents and as a chemical intermediate in the synthesis of other compounds. Despite its widespread use, there is limited information available on the potential toxicity and environmental impact of 4-(4-isopropylphenyl)butan-2-one.
Check Digit Verification of cas no
The CAS Registry Mumber 10528-64-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,2 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 10528-64:
(7*1)+(6*0)+(5*5)+(4*2)+(3*8)+(2*6)+(1*4)=80
80 % 10 = 0
So 10528-64-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H18O/c1-10(2)13-8-6-12(7-9-13)5-4-11(3)14/h6-10H,4-5H2,1-3H3
10528-64-0Relevant articles and documents
Synthesis and neuroprotective evaluation of (E)-3,4-dihydroxystyryl p-substituted-phenethyl ketone derivatives against inflammatory and oxidative injury
Cheng, Can,Ning, Xianling,Luo, Yongming,Tian, Chao,Wang, Xiaowei,Guo, Ying,Liu, Junyi,Zhang, Zhili
, p. 1678 - 1685 (2016/07/30)
(E)-3,4-dihydroxystyryl p-substituted-phenethyl ketones and their 3,4-diacetylated derivatives were synthesized and examined their neuroprotective activities to further study the effect of p-substituents on the aromatic ring. The results revealed that steric hindrance effect of p-substituents has impact on neuroprotective activities against inflammatory and oxidative injury. Introduction of the bulkier groups are more beneficial to improve the neuroprotective activities than smaller groups. Compounds (4–5h, 4–5i and 4–5e) with p-substituted trifluoromethyl, isopropyl and t-butyl groups exhibited the best effects among all the target compounds.
