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Merck
CN

29162

2-氧环己烷羧酸甲酯

technical, ≥90% (GC)

别名:

2-甲氧羰基环己酮, 环己酮-2-羧酸甲酯

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关于此项目

经验公式(希尔记法):
C8H12O3
化学文摘社编号:
分子量:
156.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
255-306-9
Beilstein/REAXYS Number:
510258
MDL number:
Assay:
≥90% (GC)
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InChI key

JEENWEAPRWGXSG-UHFFFAOYSA-N

InChI

1S/C8H12O3/c1-11-8(10)6-4-2-3-5-7(6)9/h6H,2-5H2,1H3

SMILES string

COC(=O)C1CCCCC1=O

grade

technical

assay

≥90% (GC)

refractive index

n20/D 1.483

bp

50 °C/0.2 mmHg (lit.)

density

1.10 g/mL at 20 °C (lit.)

Quality Level

Application

Methyl 2-oxocyclohexanecarboxylate has been used in the synthesis of substituted tetrahydrobenzofuran derivatives via reaction with propargylic esters in the presence of palladium catalyst.

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

192.2 °F - closed cup

flash_point_c

89 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

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分析证书(COA)

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Highly diastereoselective synthesis of tetrahydrobenzofuran derivatives by palladium-catalyzed reaction of propargylic esters with substituted ?-dicarbonyl compounds.
Yoshida M, et al.
Tetrahedron, 66(14), 2675-2682 (2010)
Qinglei Meng et al.
Nature communications, 8, 14190-14190 (2017-02-01)
Cyclohexanone and its derivatives are very important chemicals, which are currently produced mainly by oxidation of cyclohexane or alkylcyclohexane, hydrogenation of phenols, and alkylation of cyclohexanone. Here we report that bromide salt-modified Pd/C in H

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