100606-34-6 Usage
Description
(2E)-3-(4-methoxy-2-methylphenyl)-2-propenoic acid, also known as p-methoxycinnamic acid, is a phenylpropanoid chemical compound with a molecular formula of C11H12O3. It is a derivative of cinnamic acid and is commonly found in various plant species. (2E)-3-(4-methoxy-2-methylphenyl)-2-propenoic acid is recognized for its antioxidant and anti-inflammatory properties and has been studied for its potential therapeutic effects in conditions such as cardiovascular disease, diabetes, and cancer.
Uses
Used in Pharmaceutical Industry:
(2E)-3-(4-methoxy-2-methylphenyl)-2-propenoic acid is used as an active pharmaceutical ingredient for its potential therapeutic effects in treating cardiovascular disease, diabetes, and cancer due to its antioxidant and anti-inflammatory properties.
Used in Food Industry:
(2E)-3-(4-methoxy-2-methylphenyl)-2-propenoic acid is used as a food additive and flavoring agent in the food industry, contributing to the enhancement of taste and aroma in various food products.
Used in Cosmetic Industry:
In the cosmetic industry, (2E)-3-(4-methoxy-2-methylphenyl)-2-propenoic acid is utilized for its antioxidant properties, which can help in the development of skincare products that protect the skin from oxidative stress and promote overall skin health.
Check Digit Verification of cas no
The CAS Registry Mumber 100606-34-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,6,0 and 6 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 100606-34:
(8*1)+(7*0)+(6*0)+(5*6)+(4*0)+(3*6)+(2*3)+(1*4)=66
66 % 10 = 6
So 100606-34-6 is a valid CAS Registry Number.
100606-34-6Relevant articles and documents
ANTI-HIV COMPOUNDS
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Paragraph 0312, (2016/07/05)
This invention provides, among other things, tetrahydroisoquinolines useful for treating viral infections, pharmaceutical formulations containing such compounds, as well as methods of inhibiting the replication of a virus, such as HIV, or treating a disease, such as AIDS.
A concise synthesis of the naphthoic acid component of neocarzinostatin chromophore featuring a new photocyclization reaction
Myers, Andrew G.,Subramanian, Vijaya,Hammond, Marlys
, p. 587 - 590 (2007/10/02)
A 6-step synthesis of the naphthoic acid component of the natural antitumor agent neocarzinostatin chromophore is described. The synthetic route employs 4-bromo-3-methylanisole as the starting material, proceeds in 31-37% yield for the 6 steps, and featur
Organoiron Complexes in Organic Synthesis. Part 27. Synthesis and Reactivity of Tricarbonyliron Derivatives of 1,2-Disubstituted 4-Alkoxycyclohexadienylium Cations
Pearson, Anthony J.,Perrior, Trevor R.,Griffin, David A.
, p. 625 - 631 (2007/10/02)
The synthesis, and reactions with stable enolate nucleophiles, of 1,2-disubstituted 4-alkoxycyclohexadienylium(tricarbonyl)iron complexes (3a), (3b), (3c), and (3d) is described.Only the 1,2-dimethyl-4-isopropoxycyclohexadienylium complex (3b) was found to react with nucleophiles with sufficiently high regioselectivity to allow a useful method of preparation of 3,4,4-trisubstituted cyclohexenones.
