129647-84-3

Basic information

• Product Name: (2R,3S)-threo-2-phenylpentan-3-ol
• Synonyms: (2R,3S)-threo-2-phenylpentan-3-ol
• CAS NO: 129647-84-3
• Molecular Weight: 164.247
• Mol File: 129647-84-3.mol
• Article Data: 15

Chemical Properties

• CAS DataBase Reference: (2R,3S)-threo-2-phenylpentan-3-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3S)-threo-2-phenylpentan-3-ol(129647-84-3)
• EPA Substance Registry System: (2R,3S)-threo-2-phenylpentan-3-ol(129647-84-3)

Safety Data

• Hazardous Substances Data: 129647-84-3(Hazardous Substances Data)

Upstream product

• 10467-10-4 ethylmagnesium iodide 
• 34713-70-7 2-Phenylpropanal 
• 93-53-8 (S)-2-phenyl-propionaldehyde 
• 63801-22-9 2-phenylpentan-3-one 
• 2397-68-4 sodium tetraethylaluminate 
• 78-00-2 tetraethyllead(IV) 
• 557-20-0 diethylzinc 
• 925-90-6 ethylmagnesium bromide 

Downstream Products

• 24663-49-8 DL-erythro-2-Phenyl-pentyl-⁽³⁾-methansulfonat 
• 127181-69-5 (2R,3R)-erythro-2-phenylpentan-3-ol 
• 75724-23-1 cyclohexyl-2 pentanol-3 
• 75724-23-1 cyclohexyl-2 pentanol-3 
• 75724-31-1 (+/-)-threo-3-(3.5-dinitro-benzoyloxy)-2-phenyl-pentane 

Relevant articles and documents

Highly Diastereoselective 1,2-Asymmetric Addition of Dialkylzincs to Chiral 2-Phenylpropanal Catalyzed by Amino Alcohol

Diastereoselective addition of dialkylzinc reagents to 2-phenylpropanal using amino alcohol as catalyst afforded erythro alcohols (Cram-selectivity) in high diastereomeric excess (up to 88percent d.e.).

Complete regio- and stereoselectivity control in the halohydroxylation of non-activated allenes mediated by a remote sulfinyl group

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[1,2]-Wittig rearrangement of enantio-defined α-alkoxyalkyllithiums: Structural requirement and steric course at the Li-bearing terminus

The [1,2]-Wittig rearrangements of enantio-defined α-benzyloxypropyllithium and its (R)-α-methylbenzyloxy analogs, generated from the enantio-enriched stannanes via Sn/Li exchange, are shown to proceed predominantly with inversion of configuration at the