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12310

p-Benzoquinone

Name: <I>p</I>-Benzoquinone
Brand: SIAL

purum, ≥98.0% (HPLC)

Synonym(s):

Quinone

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About This Item

Linear Formula:

C₆H₄(=O)₂

CAS Number:

106-51-4

Molecular Weight:

108.09

EC Number:

203-405-2

UNSPSC Code:

12352100

MDL number:

MFCD00001591

Beilstein/REAXYS Number:

773967

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Properties

Quality Level

200

vapor density

3.73 (vs air)

vapor pressure

0.1 mmHg ( 25 °C)

grade

purum

assay

≥98.0% (HPLC)

autoignition temp.

815 °F

sublimation residue

≤1%

mp

111-114 °C, 113-115 °C (lit.)

storage temp.

2-8°C

SMILES string

O=C1C=CC(=O)C=C1

InChI

1S/C6H4O2/c7-5-1-2-6(8)4-3-5/h1-4H

InChI key

AZQWKYJCGOJGHM-UHFFFAOYSA-N

Description

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signalword

Danger

Hazard Classifications

Flam. Sol. 1

Storage Class

4.1B - Flammable solid hazardous materials

wgk

WGK 3

flash_point_f

No data available

flash_point_c

No data available

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

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Indoleamine 2,3-dioxygenase is the anticancer target for a novel series of potent naphthoquinone-based inhibitors.

Sanjeev Kumar et al.

Journal of medicinal chemistry, 51(6), 1706-1718 (2008-03-06)

Indoleamine 2,3-dioxygenase (IDO) is emerging as an important new therapeutic target for the treatment of cancer, chronic viral infections, and other diseases characterized by pathological immune suppression. While small molecule inhibitors of IDO exist, there remains a dearth of high-potency

Bioactivities of simplified adociaquinone B and naphthoquinone derivatives against Cdc25B, MKP-1, and MKP-3 phosphatases.

Shugeng Cao et al.

Bioorganic & medicinal chemistry, 17(6), 2276-2281 (2008-11-26)

Some simplified adociaquinone B analogs and a series of 1,4-naphthoquinone derivatives were synthesized and tested against the three enzymes Cdc25B, MKP-1, and MKP-3. Cdc25B and MKP-1 in particular are enzymes overexpressed in human cancer cells, and they represent potential molecular

Identification and characterization of novel benzil (diphenylethane-1,2-dione) analogues as inhibitors of mammalian carboxylesterases.

Randy M Wadkins et al.

Journal of medicinal chemistry, 48(8), 2906-2915 (2005-04-15)

Carboxylesterases (CE) are ubiquitous enzymes responsible for the metabolism of xenobiotics. Because the structural and amino acid homology among esterases of different classes, the identification of selective inhibitors of these proteins has proved problematic. Using Telik's target-related affinity profiling (TRAP)

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Global Trade Item Number

SKU	GTIN
12310-1KG-R	04061838722058
12310-6X1KG-R	04061833544365
12310-500G-R	04061838722072
12310-2.5KG-R	04061838722065