75393-93-0 Usage
Chemical Class
Phenols
Primary Use
Antioxidant in various industries (food, personal care)
Mechanism of Action
Prevents oxidation by scavenging free radicals
Chemical Composition
2,6-di-tert-butyl-4-methylphenol (BHT) group and 4-methoxyphenylmethyl group
Safety Profile
Relatively safe for use, low toxicity
Potential Skin Effects
Minimal risk of skin irritation or sensitization
Precautions
Handle and use with proper safety measures as with any chemical compound
Check Digit Verification of cas no
The CAS Registry Mumber 75393-93-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,3,9 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 75393-93:
(7*7)+(6*5)+(5*3)+(4*9)+(3*3)+(2*9)+(1*3)=160
160 % 10 = 0
So 75393-93-0 is a valid CAS Registry Number.
75393-93-0Relevant articles and documents
Thiourea catalyzed 1,6-conjugate addition of indoles to para-quinone methides
Wu, Guangmiao,Li, Tao,Liu, Fuhai,Zhao, Yulong,Ma, Shiqiang,Tang, Shouchu,Xie, Xingang,She, Xuegong
, (2021/09/09)
An efficient thiourea catalyzed 1,6-conjugate addition of indoles to para-quinone methides (p-QMs) was developed. p-QMs was activated by a weak hydrogen-bond effect. The reaction is featured mild reaction conditions and wide substrate scope. A series of C-3 bisaryl methine substituted indoles are prepared in high yield.
Synthesis of Mannich Bases of Bioactive Benzylphenols
Jurd, Leonard
, p. 81 - 83 (2007/10/02)
2,4-Bis(1,1-dimethylethyl)-6-phenol (4), prepared by oxidation of 2,4-bis(1,1-dimethylethyl)-6-phenol (1) with silver oxide in methanol, reacts with secondary amines in boiling toluene to give Manni
