19775-91-8

Basic information

• Product Name: 1-Penten-3-ol, 4,4-dimethyl-1-phenyl-, (1E)-
• CAS NO: 19775-91-8
• Molecular Formula: C13H18O
• Molecular Weight: 190.285
• Mol File: 19775-91-8.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: 1-Penten-3-ol, 4,4-dimethyl-1-phenyl-, (1E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Penten-3-ol, 4,4-dimethyl-1-phenyl-, (1E)-(19775-91-8)
• EPA Substance Registry System: 1-Penten-3-ol, 4,4-dimethyl-1-phenyl-, (1E)-(19775-91-8)

Safety Data

• Hazardous Substances Data: 19775-91-8(Hazardous Substances Data)

Upstream product

• 538-44-3 (E)-benzylidenepinacolone 
• 100-52-7 benzaldehyde 
• 75-97-8 3,3-dimethyl-butan-2-one 
• 14371-10-9 (E)-3-phenylpropenal 
• 677-22-5 tert-butylmagnesium chloride 
• 4110-75-2 (E)-(2-methoxyvinyl)benzene 
• 630-19-3 pivalaldehyde 
• 132350-97-1 4,4-dimethyl-1-phenyl-pent-1-yn-3-ol 
• 557-20-0 diethylzinc 
• 594-19-4 tert.-butyl lithium 
• 100-42-5 styrene 
• 536-74-3 phenylacetylene 

Downstream Products

• 18335-33-6 1-phenyl-4,4-dimethyl-3-pentanol 
• 1314802-09-9 1-((E)-3-azido-4,4-dimethylpent-1-enyl)-benzene 
• 1314802-25-9 (2E)-N-(4-methoxybenzyloxy)-3-(1-((E)-4,4-dimethyl-1-phenylpent-1-en-3-yl)-1H-1,2,3-triazol-4-yl)acrylamide 
• 1314801-86-9 (2E)-N-hydroxy-3-(1-((E)-4,4-dimethyl-1-phenylpent-1-en-3-yl)-1H-1,2,3-triazol-4-yl)acrylamide 
• 1401009-11-7 C₁₇H₂₇O₃PS 
• 1401009-23-1 C₁₃H₁₇F 
• 29585-96-4 1-t-Butyl-3-phenylpropyl-methylxanthogenat 
• 86429-37-0 trans-1-phenyl-4,4-dimethyl-2-pentene 
• 351536-30-6 3-tert-butyldimethylsilyloxy-2,2-dimethyl-5-phenyl-3-pentene 
• 109801-05-0 (R)-2,2-Dimethyl-1-((1S,2S)-2-phenyl-cyclopropyl)-propan-1-ol 
• 86984-00-1 (E)-3-chloro-4,4-dimethyl-1-phenylpent-1-ene 

Relevant articles and documents

Asymmetric transfer hydrogenation of cycloalkyl vinyl ketones to allylic alcohols catalyzed by ruthenium amido complexes

A chemoselective 1,2-reduction of cycloalkyl vinyl ketones via asymmetric transfer hydrogenation is described. The reduction proceeded smoothly with a chiral diamine ruthenium complex as a catalyst and a HCOOH-NEt3 azeotrope as both a hydrogen source and solvent under mild conditions. A wide range of 1-cycloalkyl chiral allylic alcohols were obtained in good yields and up to 87% ee. It was found that the alkyl group plays an important role in the enantioselectivity.

Structure-based optimization of click-based histone deacetylase inhibitors

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