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I2002

1,3-茚满二酮

Name: 1,3-茚满二酮
Brand: ALDRICH

97%

别名:

1,3-二酮氢茚

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关于此项目

经验公式（希尔记法）:

C₉H₆O₂

化学文摘社编号:

606-23-5

分子量:

146.14

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24895958

EC Number:

210-109-7

Beilstein/REAXYS Number:

1210061

MDL number:

MFCD00003779

Assay:

97%

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属性

Quality Level

200

assay

97%

mp

129-132 °C (lit.)

SMILES string

O=C1CC(=O)c2ccccc12

InChI

1S/C9H6O2/c10-8-5-9(11)7-4-2-1-3-6(7)8/h1-4H,5H2

InChI key

UHKAJLSKXBADFT-UHFFFAOYSA-N

说明

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)

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[Effect of S-oxidation on the anticoagulant effects of 4-hydroxycoumarins, 4-hydroxy-2-pyrones and 1,3-indanediones].

K Rehse et al.

Archiv der Pharmazie, 317(3), 262-267 (1984-03-01)

Organic synthesis in water: a green protocol for the synthesis of 2-(cyclohexylamino)-3- aryl- indeno[1,2-b]furan-4-ones.

Majid M Heravi et al.

Molecular diversity, 13(3), 385-387 (2009-03-03)

Aldehydes, 1,3-indandione and cyclohexylisocyanide undergo smooth coupling-cyclization in water to produce the corresponding 2-(cyclohexylamino)-3-aryl- indeno [1,2-b] furan-4-ones in good yields. Water was used as a solvent to avoid the use of other highly toxic and environmentally unfavorable solvents for this

Benzylidine indane-1,3-diones: As novel urease inhibitors; synthesis, in vitro, and in silico studies.

Bilquees Bano et al.

Bioorganic chemistry, 81, 658-671 (2018-09-27)

Current study deals with the evaluation of indane-1,3-dione based compounds as new class of urease inhibitors. For that purpose, benzylidine indane-1,3-diones (1-30) were synthesized and fully characterized by different spectroscopic techniques including EI-MS, HREI-MS, 1H, and 13C NMR. All synthetic

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全球贸易项目编号

货号	GTIN
I2002-25MG	04061832730448
I2002-250MG	04061832730431
I2002-5G-A	04061832490205
I2002-25G-A	04061833848241
I2002-100MG	04061833848234
I2002-500MG	04061832730455