20020-94-4

Basic information

• Product Name: 2,3,4,5-tetramethylbenzyl alcohol
• CAS NO: 20020-94-4
• Molecular Weight: 164.247
• Mol File: 20020-94-4.mol

Chemical Properties

• CAS DataBase Reference: 2,3,4,5-tetramethylbenzyl alcohol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,4,5-tetramethylbenzyl alcohol(20020-94-4)
• EPA Substance Registry System: 2,3,4,5-tetramethylbenzyl alcohol(20020-94-4)

Safety Data

• Hazardous Substances Data: 20020-94-4(Hazardous Substances Data)

Upstream product

• 700-12-9 pentamethylbenzene, 
• 29399-29-9 2,3,4,5-tetramethyl-benzyl chloride 
• 488-23-3 1,2,3,4-Tetramethylbenzene 
• 29344-95-4 2,3,4,5-Tetramethylbenzaldehyde 
• 509-14-8 tetranitromethane 
• 29344-90-9 2,3,4,5-Tetramethylbenzylacetat 

Downstream Products

• 873384-21-5 (2,3,4,5-tetramethyl-phenyl)-acetonitrile 
• 53546-73-9 (2,3,4,5-tetramethyl-phenyl)-acetic acid 
• 29399-29-9 2,3,4,5-tetramethyl-benzyl chloride 

Relevant articles and documents

Process for producing cyclopropanecarboxylates

There is disclosed a process process for producing a cyclopropanecarboxylate of formula (1): 1which process comprises reacting cyclopropanecarboxylic acid of formula (2): 2with a monohydroxy compound of formula (3): R6OH??(3),in the presence of a catalyst compound comprising an element of to Group 4 of the Periodic Table of Elements.

Photochemical nitration by tetranitromethane. Part XXXIV. The photochemical reactions of pentamethylbenzene and hexamethylbenzene with tetranitromethane. The formation and rearrangement of labile adducts from pentamethylbenzene

The photolysis of the charge transfer (CT) complex of tetranitromethane and Pentamethylbenzene (13) in dichloromethane at - 50 or - 78°C gives the labile epimeric 1,2,3,4,6-pentamethyl-3-nitro-6-trinitromethylcyclohexa-1,4-dienes 18 and 19. Adduct 18 rearranges rapidly in [2H2]dichloromethane at 22°C (half-life 9 min) to give 2,3,4,5-tetrarnethyl-1-(2′,2′,2′-trinitroethyl)benzene (21), 2,3,4,5-tetramethylphenylnitromethane (26), 2,3,4,5-tetramethylbenzyl nitrate (32) and 2,3,4,5-tetramethylbenzyl nitrite (36). The photolysis of the tetranitromethane-13 CT complex in dichloromethane at 20°C gives compounds 21, 26, 32 and 36, in addition to their 2,3,4,6-tetramethyl analogues 20, 25, 31 and 35, the latter set of products probably arising from the rearrangement of the highly labile epimeric 1,2,3,5,6-pentamethyl-3-nitro-6-trinitromethylcyclohexa-1,4-dienes 54. The photolysis of the tetranitromethane-13 CT complex in acetonitrile gives mainly the phenylnitromethane 26, while similar reaction in 1,1,1,3,3,3-hexafluoropropan-2-ol yields pentamethylnitrobenzene 24, the latter by a nitrosation/oxidation sequence. Reaction of 13 with nitrogen dioxide in dichloromethane gives mainly compounds 26 and 30. No adducts were detected in the photolysis of the CT complex of hexamethylbenzene 14 in dichloromethane at accessible reaction temperatures (≥ -20°C), but products of side-chain modification 37-46 were formed. In acetonitrile similar reaction gave in addition to the above products 37-46 the N-nitrosoacetamide 47 and its precursor 49. Compounds 47 and 49 are also formed, along with the major products pentamethylbenzyl nitrate 39 and the mono- and di-nitromethyl compounds 40 and 43, on reaction of 14 with nitrogen dioxide in acetonitrile. EPR spectroscopic examination of the photolysis of acidic (trifluoroacetic acid, 0.4 mol dm-3) solutions of tetranitromethane and 13 or 14 demonstrated the formation of the corresponding radical cation or a transformation product thereof, i.e. the 1,2,3,4,5,6,7,8-octamethylanthracene radical cation from 13 or 14·+ from 14. Acta Chemica Scandinavica 1996.