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Merck
CN

410772

3-羰基-1-茚酸

98%

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关于此项目

经验公式(希尔记法):
C10H8O3
化学文摘社编号:
分子量:
176.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
98%
Form:
solid
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assay

98%

form

solid

mp

111-113 °C (lit.)

functional group

carboxylic acid, ketone

SMILES string

OC(=O)C1CC(=O)c2ccccc12

InChI

1S/C10H8O3/c11-9-5-8(10(12)13)6-3-1-2-4-7(6)9/h1-4,8H,5H2,(H,12,13)

InChI key

HXLJFMRZKCSTQD-UHFFFAOYSA-N

General description

3-Oxo-1-indancarboxylic acid participates in the synthesis of 3-hydroxymethyl-1-indanol (±). Enantiomeric separation of 3-oxo-1-indancarboxylic acid on liquid chromatography chiral stationary phases (CSPs) by supercritical fluid chromatography (SFC) has been reported. Separation of 3-oxo-1-indancarboxylic acid enantiomers using a new immobilized polysaccharide chiral stationary phase, CHIRALPAK IA with hexane has been described.


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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Extending the Range of Solvents for Chiral Analysis Using a New Immobilized Polysaccharide Chiral Stationary Phase, CHIRALPAK IA.
Cox GB and Amoss CW.
LCGC North America, 22(2), 32-32 (2004)
Kinetic resolution of 3-hydroxymethylbenzocycloalkanols by selective asymmetric hydrogen-transfer oxidation.
Caro Y, et al.
Tetrahedron Asymmetry, 14(23), 3689-3696 (2003)
Super/subcritical fluid chromatography separations with four synthetic polymeric chiral stationary phases.
Han X, et al.
Chromatographia, 65(7-8), 381-400 (2007)



全球贸易项目编号

货号GTIN
410772-10G04061831810837
410772-1G04061825585079