101980-92-1

Basic information

• Product Name: αH-4-(acetoxymethyl)tetradecachlorotriphenylmethane
• Synonyms: αH-4-(acetoxymethyl)tetradecachlorotriphenylmethane
• CAS NO: 101980-92-1
• Molecular Weight: 798.63
• Mol File: 101980-92-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: αH-4-(acetoxymethyl)tetradecachlorotriphenylmethane(CAS DataBase Reference)
• NIST Chemistry Reference: αH-4-(acetoxymethyl)tetradecachlorotriphenylmethane(101980-92-1)
• EPA Substance Registry System: αH-4-(acetoxymethyl)tetradecachlorotriphenylmethane(101980-92-1)

Safety Data

• Hazardous Substances Data: 101980-92-1(Hazardous Substances Data)

Upstream product

• 79839-38-6 6,6’-((2,3,5,6-tetrachloro-4-methylphenyl)methylene)bis(1,2,3,4,5-pentachlorobenzene) 
• 127-09-3 sodium acetate 
• 81221-80-9 4-(bromomethyl)tetradecachlorotriphenylmethyl radical 
• 101998-20-3 6,6'-((4-(bromomethyl)-2,3,5,6-tetrachlorophenyl)methylene)bis(1,2,3,4,5-pentachlorobenzene) 

Downstream Products

• 101980-98-7 2,3,5,6-tetrachloro-4-(bis(pentachlorophenyl)methyl)-α-hydroxytoluene 
• 85632-68-4 1,2-ethylenebis(4-tetradecachlorotriphenylmethyl) diradical 
• 101981-02-6 αH-tetradecachloro-4-(chloromethyl)triphenylmethane 
• 101980-95-4 αH-tetradecachloro-4-(cyanomethyl)triphenylmethane 
• 101980-99-8 αH-tetradecachloro-4-formyltriphenylmethane 
• 101981-04-8 tetradecachloro-4-(hydroxymethyl)triphenylmethyl radical 
• 101981-00-4 αH-4-(carboxymethyl)tetradecachlorotriphenylmethane 
• 101981-01-5 αH-4-(2-carboxyethyl)tetradecachlorotriphenylmethane 
• 101981-09-3 tetradecachloro-4-(2-(chlorocarbonyl)ethyl)triphenylmethyl radical 
• 101981-05-9 4-(2-carboxyethyl)tetradecachlorotriphenylmethyl radical 
• 101980-93-2 2,3,5,6-tetrachloro-4-(bis(pentachlorophenyl)methyl)-α-(tosyloxy)toluene 
• 101980-96-5 αH-tetradecachloro-4-(2,2-bis(ethoxycarbonyl)ethyl)triphenylmethane 
• 101981-03-7 αH-4-(2-(alaninocarbonyl)ethyl)tetradecachlorotriphenylmethane ethyl ester 
• 101981-10-6 4-(2-(alaninocarbonyl)ethyl)tetradecachlorotriphenylmethyl radical ethyl ester 

Relevant articles and documents

Inert Carbon Free Radicals. 7. "The (Kinetic) Reverse Effect" and Relevant Synthesis of New Monofunctionalized Triphenylmethyl Radicals and Their Nonradical Counterparts

The high chemical passivity of the so-called "inert free radicals" (IFRs), particularly those derived from perchlorotriphenylmethyl (PTM), has allowed one to ascertain the kinetic influence of the free radical character on the reactivity of their nonradic