登录 查看组织和合同定价。
选择尺寸
变更视图
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)
grade
technical
Quality Level
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.)
SMILES string
COC(=O)C1CCCCC1=O
InChI
1S/C8H12O3/c1-11-8(10)6-4-2-3-5-7(6)9/h6H,2-5H2,1H3
InChI key
JEENWEAPRWGXSG-UHFFFAOYSA-N
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
新产品
此项目有
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
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 29162-50ML | 04061836691820 |
| 29162-10ML | 04061836691813 |