13058-13-4 Usage
Uses
Used in Pharmaceutical Industry:
3-(2,3,4-Trihydroxy-phenyl)propionic acid is used as a pharmaceutical compound for its potential health benefits, including anti-inflammatory, anti-cancer, and neuroprotective effects. Its antioxidant properties contribute to its therapeutic potential in various medical applications.
Used in Nutraceutical Industry:
In the nutraceutical industry, 3-(2,3,4-Trihydroxy-phenyl)propionic acid is used as a dietary supplement or functional ingredient in health products due to its antioxidant and health-promoting properties. It can be incorporated into formulations to support overall well-being and address specific health concerns.
Used in Cosmetic Industry:
3-(2,3,4-Trihydroxy-phenyl)propionic acid is used in the cosmetic industry as an active ingredient in skincare and beauty products. Its antioxidant and anti-inflammatory properties can contribute to skin health, protection, and rejuvenation, making it suitable for various cosmetic formulations.
Used in Food and Beverage Industry:
In the food and beverage industry, 3-(2,3,4-Trihydroxy-phenyl)propionic acid can be used as a natural preservative or flavor enhancer due to its antioxidant properties. It can help extend the shelf life of food products and improve their taste and nutritional value.
Used in Agricultural Industry:
3-(2,3,4-Trihydroxy-phenyl)propionic acid can be used in the agricultural industry as a natural pesticide or growth promoter. Its antioxidant and anti-inflammatory properties may help protect crops from diseases and enhance their growth and yield.
Overall, 3-(2,3,4-Trihydroxy-phenyl)propionic acid is a versatile compound with potential applications across various industries, including pharmaceutical, nutraceutical, cosmetic, food and beverage, and agricultural sectors. Its health benefits and antioxidant properties make it a promising candidate for further research and development in natural medicine and other fields.
Check Digit Verification of cas no
The CAS Registry Mumber 13058-13-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,5 and 8 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13058-13:
(7*1)+(6*3)+(5*0)+(4*5)+(3*8)+(2*1)+(1*3)=74
74 % 10 = 4
So 13058-13-4 is a valid CAS Registry Number.
13058-13-4Relevant academic research and scientific papers
Contribution of cinnamic acid analogues in rosmarinic acid to inhibition of snake venom induced hemorrhage
Aung, Hnin Thanda,Furukawa, Tadashi,Nikai, Toshiaki,Niwa, Masatake,Takaya, Yoshiaki
experimental part, p. 2392 - 2396 (2011/05/12)
In our previous paper, we reported that rosmarinic acid (1) of Argusia argentea could neutralize snake venom induced hemorrhagic action. Rosmarinic acid (1) consists of two phenylpropanoids: caffeic acid (2) and 3-(3,4-dihydroxyphenyl)lactic acid (3). In this study, we investigated the structural requirements necessary for inhibition of snake venom activity through the use of compounds, which are structurally related to rosmarinic acid (1). By examining anti-hemorrhagic activity of cinnamic acid analogs against Protobothrops flavoviridis (Habu) venom, it was revealed that the presence of the E-enoic acid moiety (-CHCH-COOH) was critical. Furthermore, among the compound tested, it was concluded that rosmarinic acid (1) (IC50 0.15 μM) was the most potent inhibitor against the venom.
Synthesis of diverse analogues of Oenostacin and their antibacterial activities
Srivastava, Vandana,Darokar, Mahendra P.,Fatima, Atiya,Kumar,Chowdhury, Chinmay,Saxena, Hari Om,Dwivedi, Gaurav R.,Shrivastava, Kunal,Gupta, Vivek,Chattopadhyay,Luqman, Suaib,Gupta,Negi, Arvind S.,Khanuja, Suman P.S.
, p. 518 - 525 (2008/03/12)
Several diverse analogues of Oenostacin, a naturally occurring potent antibacterial phenolic acid derivative, have been synthesized. A small library with more than forty analogues having different aromatic rings and varied side chains has been achieved through solution phase synthesis. Some of these analogues, that is, 22, 23 and 42, possessed potent antibacterial activities against Staphylococcus epidermidis and Staphylococcus aureus having EC50 ranging from 0.49 to 0.67 μM as compared to Oenostacin (EC50 = 0.12 μM).
