4-Phenyl-3-butyn-2-one, 96%

Name: 4-Phenyl-3-butyn-2-one, 96%
SKU: H27826.03

CAS: 1817-57-8 | C10H8O | 144.173 g/mol

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数量:

1 g

5 g

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製品番号（カタログ番号） H27826.03

または、製品番号H27826-03

価格（JPY）

数量:

1 g

一括またはカスタム形式をリクエストする

化学物質識別子

CAS1817-57-8

IUPAC Name4-phenylbut-3-yn-2-one

Molecular FormulaC10H8O

InChI KeyUPEUQDJSUFHFQP-UHFFFAOYSA-N

SMILESCC(=O)C#CC1=CC=CC=C1

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仕様

スペックシート

Identification (FTIR)Conforms

Refractive Index1.5710-1.5770 @ 20?C

FormLiquid

Appearance (Color)Clear colorless to yellow

Assay (GC)≥95.0%

It is used as pharmaceutical intermediate.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
It is used as pharmaceutical intermediate.

Solubility
Insoluble in water.

Notes
Store in cool dry conditions. Incompatible with oxidizing agents.

RUO – Research Use Only

General References:

P.Veeraraghavan Ramachandran.; Baoqing Gong.; Aleksandar V. Teodorovic'.; Herbert C. Brown. Selective reductions. 52. Efficient asymmetric reduction of α-acetylenic α'-fluoroalkyl ketones with either B-chlorodiisopinocampheylborane or B-isopinocampheyl-9-borabicyclo[3.3.1]nonane in high enantiomeric purity. The influence of fluoro groups in such reductions.Tetrahedron: Asymmetry. 1994, 5 (6),1061-1074 .
M. Mark Midland.; Deborah C. McDowell.; Robert L. Hatch.; Alfonso Tramontano. Reduction of .alpha.,.beta.-acetylenic ketones with B-3-pinanyl-9-borabicyclo[3.3.1]nonane. High asymmetric induction in aliphatic systems.J. Am. Chem. Soc. 1980, 102 (2),867-869 .