33538-75-9 Usage
Chemical family
Phenol 2-(3-hydroxypropyl)-4-methylphenol belongs to the phenol family of compounds.
Industrial applications
Stabilizer for polymers 2-(3-hydroxypropyl)-4-methylphenol helps maintain the stability and integrity of certain polymers.
Pharmaceutical production
Used in the production of pharmaceuticals This chemical is utilized in the synthesis of various pharmaceutical drugs.
Fragrance ingredient
Cosmetic and personal care products 2-(3-hydroxypropyl)-4-methylphenol is used as a fragrance component in cosmetics and personal care items.
Potential medical properties
Anti-inflammatory Research has shown that this chemical may possess anti-inflammatory properties, which could be beneficial in treating inflammation-related conditions.
Potential medical properties
Anti-cancer 2-(3-hydroxypropyl)-4-methylphenol has demonstrated potential anti-cancer properties, making it a subject of interest for further research and development in the medical and pharmaceutical fields.
Check Digit Verification of cas no
The CAS Registry Mumber 33538-75-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,5,3 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 33538-75:
(7*3)+(6*3)+(5*5)+(4*3)+(3*8)+(2*7)+(1*5)=119
119 % 10 = 9
So 33538-75-9 is a valid CAS Registry Number.
33538-75-9Relevant academic research and scientific papers
SYNTHETIC METHODS
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Page/Page column 48, (2012/06/16)
New strategies for the synthesis of salicylaldehyde derivatives having utility production of catalytic metal complexes.
Synthetic and Stereochemical Studies of the Octahydro-1-benzopyran System
Griffiths, D. Vaughan,Wilcox, Geoffrey
, p. 431 - 436 (2007/10/02)
The cis and trans isomers of the octahydro-1-benzopyran system have been synthesised and their conformations studied by low-temperature (13)C and highfield (1)H n.m.r. spectroscopy.The position of the conformational equilibrium in the cis isomer at -70 deg C in CDCl3-CFCl3 (50:50) has been determined as approximately 99.5:0.5 (ΔG0 -8.9 kJ mol-1) in favour of the conformation having the oxygen axially disposed towards the cyclohexane ring.
