1401998-95-5

Basic information

• Product Name: (R,E)-4,4-difluoro-1-phenylhexa-1,5-dien-3-ol
• Synonyms: (R,E)-4,4-difluoro-1-phenylhexa-1,5-dien-3-ol
• CAS NO: 1401998-95-5
• Molecular Weight: 210.223
• Mol File: 1401998-95-5.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (R,E)-4,4-difluoro-1-phenylhexa-1,5-dien-3-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (R,E)-4,4-difluoro-1-phenylhexa-1,5-dien-3-ol(1401998-95-5)
• EPA Substance Registry System: (R,E)-4,4-difluoro-1-phenylhexa-1,5-dien-3-ol(1401998-95-5)

Safety Data

• Hazardous Substances Data: 1401998-95-5(Hazardous Substances Data)

Upstream product

• 108-05-4 vinyl acetate 
• 88257-89-0 (1E)-4,4-difluoro-1-phenylhexa-1,5-dien-3-ol 
• 14371-10-9 (E)-3-phenylpropenal 
• 430-64-8 1,1-difluoroallene 
• 21932-54-7 diisopinocampheylborane 

Downstream Products

• 1415354-92-5 (1S,2E)-4,4-difluoro-1-phenylhexa-2,5-dien-1-amine 
• 1415354-91-4 C₁₄H₁₂Cl₃F₂NO 

Relevant articles and documents

Synthesis of γ-fluoroalkylated allylic amines derivatives via palladium-catalyzed Overman rearrangement

A Pd-catalyzed Overman rearrangement of α-fluoroalkylated allylic trichloroacetimidates has been developed. This reaction allows for an efficient synthesis of γ-fluoroalkylated allylic amine derivatives with excellent regio- and stereo-selectivities under

B -(3,3-Difluoroallyl)diisopinocampheylborane for the enantioselective fluoroallylboration of aldehydes

The fluoroallylboration of aldehydes with B-(3,3-difluoroallyl) diisopinocampheylborane, which was prepared via the hydroboration of 1,1-difluoroallene, provides chiral 2,2-gem-difluorinated homoallylic alcohols in good yields and 91-97% ee.