36438-63-8

Basic information

• Product Name: Benzenemethanol, a-methyl-4-(phenylmethoxy)-
• CAS NO: 36438-63-8
• Molecular Formula: C15H16O2
• Molecular Weight: 228.291
• Mol File: 36438-63-8.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, a-methyl-4-(phenylmethoxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, a-methyl-4-(phenylmethoxy)-(36438-63-8)
• EPA Substance Registry System: Benzenemethanol, a-methyl-4-(phenylmethoxy)-(36438-63-8)

Safety Data

• Hazardous Substances Data: 36438-63-8(Hazardous Substances Data)

Upstream product

• 54696-05-8 4'-benzyloxy-acetophenone 
• 100-39-0 benzyl bromide 
• 99-93-4 4-Hydroxyacetophenone 
• 100-51-6 benzyl alcohol 
• 56441-91-9 1-(benzyloxy)-4-ethylbenzene 
• 100-44-7 benzyl chloride 
• 123-08-0 4-hydroxy-benzaldehyde 
• 4397-53-9 p-benzyloxybenzaldehyde 
• 75-16-1 methylmagnesium bromide 
• 36438-64-9 p-benzyloxystyrene 

Downstream Products

• 36438-64-9 p-benzyloxystyrene 
• 670274-68-7 4-[1-(4-benzyloxy-phenyl)-ethoxy]-benzaldehyde 
• 120342-67-8 1-(1-azidoethyl)-4-(benzyloxy)benzene 
• 140685-78-5 1-(4-(benzyloxy)phenyl)-3-methylbutan-1-one 
• 154479-32-0 1-(4-(benzyloxy)phenyl)-3-phenylpropan-1-one 
• 347174-36-1 1-(4-(benzyloxy)phenyl)-2-cyclohexylethan-1-one 
• 54696-05-8 4'-benzyloxy-acetophenone 
• 103-16-2 4-Benzyloxyphenol 
• 6311-66-6 4-(benzyloxy)phenyl acetate 
• 4254-67-5 2-bromo-1-(4-benzyloxyphenyl)-1-ethanone 
• 1166901-37-6 C₂₅H₂₂O₂ 
• 1172119-84-4 1-(benzyloxy)-4-(4-bromo-4-phenylbut-3-en-2-yl)benzene 

Relevant articles and documents

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HETEROCYCLIC COMPOUNDS AS MUTANT IDH INHIBITORS

The present disclosure relates generally to compounds useful in treatment of conditions associated with mutant isocitrate dehydrogenase (mt-IDH), particularly mutant IDH1 enzymes. Specifically, the present invention discloses compound of formula (IA), which exhibits inhibitory activity against mutant IDH1 enzymes. Method of treating conditions associated with excessive activity of mutant IDH1 enzymes with such compound is disclosed. Uses thereof, pharmaceutical composition, and kits are also disclosed.

Chemoenzymatic synthesis of enantiopure 1-phenyl-2-haloethanols and their esters

Several secondary haloalcohols have been resolved by esterification catalyzed by lipases A and B from Candida antarctica (CALA and CALB, respectively). Immobilized CALB (Novozym 435) gave better selectivities and faster reaction rates than CALA (Novozyme