4670-09-1 Usage
Description
3,5-Dihydroxyphenylacetic acid, also known as DHPA, is an organic compound that plays a significant role in various biological processes and has potential applications in the pharmaceutical and chemical industries. It is characterized by the presence of two hydroxyl groups at the 3rd and 5th positions of the phenylacetic acid molecule, which allows it to participate in various chemical reactions and interactions.
Uses
Used in Pharmaceutical Industry:
3,5-Dihydroxyphenylacetic acid is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique chemical structure makes it a valuable building block for the development of new drugs with potential therapeutic applications.
Used in Neuroprotective Agents:
3,5-Dihydroxyphenylacetic acid is involved in the discovery of KLS-13019, a cannabidiol-derived neuroprotective agent. 3,5-Dihdyroxyphenylacetic acid has shown potential in protecting neurons from damage and may be useful in the treatment of neurodegenerative diseases.
Used in Metabolite Research:
As a major metabolite of myricetin, 3,5-dihydroxyphenylacetic acid is relevant in the study of the metabolic pathways and biological effects of this flavonoid. Myricetin is a naturally occurring compound found in various fruits and vegetables, and it has been linked to several health benefits, including antioxidant and anti-inflammatory properties.
Check Digit Verification of cas no
The CAS Registry Mumber 4670-09-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,7 and 0 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4670-09:
(6*4)+(5*6)+(4*7)+(3*0)+(2*0)+(1*9)=91
91 % 10 = 1
So 4670-09-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H8O4/c9-6-1-5(3-8(11)12)2-7(10)4-6/h1-2,4,9-10H,3H2,(H,11,12)
4670-09-1Relevant articles and documents
Winkler,Whetstone
, p. 784 (1961)
Preparation and application of (Z)-3,5-dihydroxy-4-isopropylstilbene
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Paragraph 0031; 0047-0056, (2021/02/24)
The invention discloses a preparation method and application of (Z)-3,5-dihydroxy-4-isopropylstilbene. According to the preparation method, a raw material, namely 3,5-dihydroxy-2,4-diethoxycarbonyl ethyl phenylacetate as an initiator, hydrolysis decarboxy
First total synthesis of medicinally important 3,4,7-trimethoxy-9,10-dihydrophenanthrene-1,5-diol
Gangireddy Venkata, Sivarami Reddy,Narkhede, Umesh C.,Jadhav, Vinod D.,Gangu Naidu, Ch.
, p. 1670 - 1673 (2018/03/29)
The first total synthesis was successfully achieved for biologically active 9,10-dihydrophenanthrene-1,5-diol. The key features of our synthetic approach are Perkin condensation, followed by bromination, palladium mediated intramolecular C-C bond coupling, and selective isopropyl ether cleavage. Synthesized compounds were purified and characterized by IR, 1HNMR, 13CNMR and HRMS/LC-MS.
