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About This Item
Empirical Formula (Hill Notation):
C13H11N
CAS Number:
Molecular Weight:
181.23
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-817-8
Beilstein/REAXYS Number:
1945861
MDL number:
Assay:
98%
Form:
powder
Quality Level
assay
98%
form
powder
mp
124-128 °C (lit.)
SMILES string
Nc1ccc-2c(Cc3ccccc-23)c1
InChI
1S/C13H11N/c14-11-5-6-13-10(8-11)7-9-3-1-2-4-12(9)13/h1-6,8H,7,14H2
InChI key
CFRFHWQYWJMEJN-UHFFFAOYSA-N
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Related Categories
signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 2 - Carc. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Prabhjit Kaur et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 48(1), 320-325 (2009-10-27)
Rubia cordifolia L. (Rubiaceae) is an important medicinal plant used in the Ayurvedic medicinal system. Its use as a traditional therapeutic has been related to the treatment of skin disorders and cancer. Besides its medicinal value, anthraquinones from this plant
E Miadokova et al.
Phytotherapy research : PTR, 22(1), 77-81 (2007-08-29)
The extract of artichoke Cynara cardunculus L. (CCE) was investigated for its potential antigenotoxic and antioxidant effects using four experimental model systems. In the Saccharomyces cerevisiae mutagenicity/antimutagenicity assay, CCE significantly reduced the frequency of 4-nitroquinoline-N-oxide-induced revertants at the ilv1 locus
Jun Zhao et al.
Stem cell research & therapy, 10(1), 165-165 (2019-06-15)
Mounting evidence has shown that a novel subset of mesenchymal stem cells (MSCs) derived from human gingiva referred to as gingival mesenchymal stem cells (GMSCs) displays a greater immunotherapeutic potential and regenerative repair expression than MSCs obtained from other tissues.
Ali Bilici et al.
Biomacromolecules, 11(10), 2593-2601 (2010-09-08)
In this paper, the results on horseradish peroxidase (HRP)-catalyzed oxidative polymerization of amine-functionalized fluorene monomer, 2-amino fluorene (AF), are reported. The resulting polymer exhibits an exciting molecular structure and spectral properties. FT-IR and NMR studies show that the two fluorene
Olga Rechkoblit et al.
Nature structural & molecular biology, 17(3), 379-388 (2010-02-16)
The aromatic amine carcinogen 2-aminofluorene (AF) forms covalent adducts with DNA, predominantly with guanine at the C8 position. Such lesions are bypassed by Y-family polymerases such as Dpo4 via error-free and error-prone mechanisms. We show that Dpo4 catalyzes elongation from
Global Trade Item Number
| SKU | GTIN |
|---|---|
| A55500-5G | 04061833376041 |
| A55500-25G | 04061833376034 |
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