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Merck
CN

362069

1,3-二苯甲酰基丙烷

98%

别名:

1,5-二苯基-1,5-戊二酮

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关于此项目

线性分子式:
C6H5CO(CH2)3COC6H5
化学文摘社编号:
分子量:
252.31
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
98%
Form:
solid
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assay

98%

form

solid

mp

66-68 °C (lit.)

functional group

ketone, phenyl

SMILES string

O=C(CCCC(=O)c1ccccc1)c2ccccc2

InChI

1S/C17H16O2/c18-16(14-8-3-1-4-9-14)12-7-13-17(19)15-10-5-2-6-11-15/h1-6,8-11H,7,12-13H2

InChI key

YOLLTWVIOASMFW-UHFFFAOYSA-N

General description

1,3-Dibenzoylpropane is a 1,3-diaroylpropane. 1,3-Dibenzoylpropane is formed during hydroxocobalt(III) Schiff base complexes catalyzed selective aldol reaction of dibenzoylmethanes with formaldehyde in methanol.

Application

1,3-Dibenzoylpropane may be used in the electrochemical synthesis of cis-1,2-diphenyl-1,2-cyclopentanediol, via reduction in acetonitrile.


存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Electrochemical cyclization: II. Intramolecular pinacolization of 1, 3-dibenzoylpropane in acetonitrile.
Ammar F, et al.
J. Electroanal. Chem. Interfac. Electrochem., 53(3), 407-416 (1974)
Highly selective aldol reaction of dibenzoylmethanes with formaldehyde catalyzed by cobalt Schiff base complex under neutral conditions.
Maruyama K, et al.
Tetrahedron Letters, 36(31), 5609-5612 (1995)



全球贸易项目编号

货号GTIN
362069-5G04061831810684