14235-77-9 Usage
General Description
3-(hydroxymethyl)pyrocatechol, also known as hydroxyacetylcatechol or 3,4-dihydroxybenzyl alcohol, is a chemical compound that is commonly used in the pharmaceutical and cosmetic industries. It is a derivative of pyrocatechol, which is a catecholamine that acts as a neurotransmitter and hormone in the human body. 3-(hydroxymethyl)pyrocatechol has been found to have antioxidant and skin whitening properties, making it a popular ingredient in skincare products. It is also being studied for its potential neuroprotective effects and applications in the treatment of neurodegenerative diseases. With its versatile applications and potential health benefits, 3-(hydroxymethyl)pyrocatechol continues to be an area of interest for researchers and industry professionals alike.
Check Digit Verification of cas no
The CAS Registry Mumber 14235-77-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,3 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14235-77:
(7*1)+(6*4)+(5*2)+(4*3)+(3*5)+(2*7)+(1*7)=89
89 % 10 = 9
So 14235-77-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H8O3/c8-4-5-2-1-3-6(9)7(5)10/h1-3,8-10H,4H2
14235-77-9Relevant articles and documents
Ionene-bound borohydrides: Efficient, selective, and versatile polymer-supported reducing agents
Lakouraj, Moslem M.,Tajbakhsh, Mahmood,Mahalli, Majid S.
, p. 117 - 123 (2008)
Reduction of structurally different carbonyl compounds, such as aldehydes, ketones, α,β-unsaturated enals and enones, acid chlorides, and imines was accomplished efficiently using high capacity ionene based borohydride reagents. Aldehydes and imines were reduced to the corresponding alcohols and amines in excellent yields in methanol at ambient temperature while ketones and acid chlorides were reduced in iso-propanol and THF-MeOH at reflux. Chemoselective reduction of aldehydes over ketones was achieved successfully with these reagents. Complete regioselectivity was also observed in the reduction of α,β-unsaturated aldehydes and ketones.
