133447-23-1 Usage
Structure
A derivative of hydroquinone (1,4-benzenediol) with a methyl group at the 2nd position and an isopropyl group at the 6th position.
Functional Groups
Two hydroxyl (-OH) groups, a methyl group (-CH3), and an isopropyl group ((CH3)2CH-)
Appearance
Likely a solid or crystalline substance, though specific appearance is not provided.
Applications
a. Antioxidant
b. Anti-inflammatory
c. Treatment of acne
d. Treatment of hyperpigmentation
Safety Precautions
Handle with caution and follow safety guidelines due to potential health and environmental hazards.
Industrial and Pharmaceutical Uses
Utilized in various industrial and pharmaceutical applications, likely related to its antioxidant, anti-inflammatory, and therapeutic properties.
Chemical Family
Aromatic diols, specifically a derivative of hydroquinone.
Check Digit Verification of cas no
The CAS Registry Mumber 133447-23-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,4,4 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 133447-23:
(8*1)+(7*3)+(6*3)+(5*4)+(4*4)+(3*7)+(2*2)+(1*3)=111
111 % 10 = 1
So 133447-23-1 is a valid CAS Registry Number.
133447-23-1Relevant articles and documents
Spiro derivatives as lipoxygenase inhibitors
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Page/Page column 90, (2008/06/13)
The present invention is concerned with certain novel spiro substituted heterocylic ring derivatives. These compounds may be useful in the manufacture of pharmaceutical compositions for treating disorders mediated by lipoxygenases. They may also be useful
Synthesis of a novel class of water-soluble and bioavailable antioxidants: 5-Hydroxycoumaran derivatives possessing imidazole group
Hasegawa, Tomoyuki,Yoshida, Koji,Hachiya, Katsutoshi,Miyazaki, Makoto,Tsuruta, Hiroshi,Nambu, Fumio,Ohuchida, Shuichi,Kawamura, Masanori
, p. 511 - 512 (2007/10/03)
The 5-hydroxycoumaran derivative 1 possessing imidazole group was synthesized from 2-isopropyl-6-methylphenol with high regioselectivity. The compound 1 was the water-soluble antioxidant with potent bioavailability and showed TXA2 synthase inhibition.
