79907-49-6

Basic information

• Product Name: 2-HYDROXYMETHYL-2,5,7,8-TETRAMETHYLCHROMAN-6-OL
• Synonyms: 2-HYDROXYMETHYL-2,5,7,8-TETRAMETHYLCHROMAN-6-OL
• CAS NO: 79907-49-6
• Molecular Formula: C₁₄H₂₀O₃
• Molecular Weight: 236.31
• Mol File: 79907-49-6.mol
• Article Data: 19

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-HYDROXYMETHYL-2,5,7,8-TETRAMETHYLCHROMAN-6-OL(CAS DataBase Reference)
• NIST Chemistry Reference: 2-HYDROXYMETHYL-2,5,7,8-TETRAMETHYLCHROMAN-6-OL(79907-49-6)
• EPA Substance Registry System: 2-HYDROXYMETHYL-2,5,7,8-TETRAMETHYLCHROMAN-6-OL(79907-49-6)

Safety Data

• Hazardous Substances Data: 79907-49-6(Hazardous Substances Data)

Upstream product

• 56305-04-5 trolox 
• 697-82-5 2,3,5-trimethylphenol 
• 700-13-0 Trimethylhydroquinone 
• 210174-90-6 methyl-6-(benzyloxy)-2,5,7,8-tetramethyl-3,4-dihydro-2H-chromene-2-carboxylate 
• 86646-83-5 methyl 6-hydroxy-2,5,7,8-tetramethylchroman-2-carboxylate 
• 171270-07-8 (6-Benzyloxy-3,4-dihydro-2,5,7,8-tetramethyl-2H-1-benzopyran-2-yl)methanol 
• 53174-07-5 ethyl 6-hydroxy-2,5,7,8-tetramethyl-3,4-dihydro-2H-chromene-2-carboxylate 
• 71490-88-5 2,3,4,5-tetrahydro-3,6,8,9-tetramethyl-1-benzoxepin-3,7-diol 

Downstream Products

• 171270-07-8 (6-Benzyloxy-3,4-dihydro-2,5,7,8-tetramethyl-2H-1-benzopyran-2-yl)methanol 
• 215597-29-8 (S)-2,6-Bis-benzyloxycarbonylamino-hexanoic acid 2-hydroxymethyl-2,5,7,8-tetramethyl-chroman-6-yl ester 
• 219653-63-1 (S)-2-(2-Benzoyl-phenylamino)-3-[4-(6-hydroxy-2,5,7,8-tetramethyl-chroman-2-ylmethoxy)-phenyl]-propionic acid methyl ester 
• 1268259-49-9 5-(4-(6-(2-(2-(2-(tert-butoxycarbonylamino)ethoxy)ethoxy)ethoxy)-2,5,7,8-tetramethylchroman-2-ylmethoxy)phenylmethylene)thiazolidine-2,4-dione 
• 1268259-50-2 5-(4-(6-(2-(2-(2-(tert-butoxycarbonylamino)ethoxy)ethoxy)ethoxy)-2,5,7,8-tetramethylchroman-2-ylmethoxy)phenylmethyl)thiazolidine-2,4-dione 
• 1268259-51-3 C₄₀H₅₄N₄O₉S₂ 
• 1268259-48-8 4-(6-(2-(2-(2-(tert-Butoxycarbonylamino)ethoxy)ethoxy)ethoxy)-2,5,7,8-tetramethylchroman-2-ylmethoxy)benzaldehyde 
• 69371-87-5 (S)-(-)-6-benzyloxy-2,5,7,8-tetramethyl-3,4-dihydro-2H-1-benzopyran-2-ylmethanol 
• 906079-28-5 (S)-[3,4-dihydro-6-benzyloxy-2,5,7,8-tetramethyl-2H-1-benzopyran-2-yl]methyl trifluoromethane-sulfonate 
• 97323-02-9 5-[4-(2,5,7,8-tetramethyl-6-nicotinoyloxychroman-2-ylmethoxy)benzyl]thiazolidine-2,4-dione 
• 97323-01-8 5-[4-(6-benzoyloxy-2,5,7,8-tetramethylchroman-2-ylmethoxy)benzyl]thiazolidine-2,4-dione 
• 97323-00-7 5-[4-(6-butyryloxy-2,5,7,8-tetramethylchroman-2-ylmethoxy)benzyl]thiazolidine-2,4-dione 
• 97322-68-4 Ethyl 3-<4-<(6-acetoxy-2,5,7,8-tetramethylchroman-2-yl)methoxy>phenyl>-2-chloropropionate 

Relevant articles and documents

THE ACID-CATALYSED RING CONTRACTION OF TETRAHYDRO-1-BENZOXEPIN-3-OL TO 2-HYDROXYMETHYLCHROMAN DERIVATIVES.

Derivatives of 2,3,4,5-tetrahydro-3-methyl-1-benzoxepin-3-ol are readily isomerised by acids into the corresponding derivatives of 2-hydroxymethyl-2-methyl chroman.

Nitrone derivatives of trolox as neuroprotective agents

Synthesis of nitrone derivatives of trolox is described. Their biological evaluation was performed in vitro for scavenging different free radicals, inhibiting Fe2+-induced lipid peroxidation, and in vivo in a permanent middle cerebral artery occlusion model in mice. New compounds exert pharmacological activities comparable to or better than those of trolox or nitrone-type reference compounds.

Trolox alcohol ester derivative, and preparation method and application thereof

The invention provides a Trolox alcohol ester derivative, and a preparation method and an application thereof, and belongs to the technical field of medicines. A carboxyl groups in Trolox is reduced into hydroxyl, then the hydroxyl group is modified, and

DEUTERATED EPI-743

This invention relates to novel α-tocotrienol quinones of Formula I: (I), and pharmaceutically acceptable salts thereof. This invention also provides compositions comprising a compound of this invention and the use of such compositions in methods of treat