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About This Item
Empirical Formula (Hill Notation):
C9H7NO
CAS Number:
Molecular Weight:
145.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-732-1
Beilstein/REAXYS Number:
2954
MDL number:
Assay:
98%
Form:
solid
Quality Level
assay
98%
form
solid
mp
211-214 °C (lit.)
SMILES string
Oc1nccc2ccccc12.O=C3NC=Cc4ccccc34
InChI
1S/C9H7NO/c11-9-8-4-2-1-3-7(8)5-6-10-9/h1-6H,(H,10,11)
InChI key
VDBNYAPERZTOOF-UHFFFAOYSA-N
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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Luca Palazzo et al.
Open biology, 9(4), 190041-190041 (2019-04-18)
ADP-ribosylation (ADPr) is a reversible post-translational modification of proteins, which controls major cellular and biological processes, including DNA damage repair, cell proliferation and differentiation, metabolism, stress and immune responses. In order to maintain the cellular homeostasis, diverse ADP-ribosyl transferases and
M Berger et al.
Nucleic acids research, 28(15), 2911-2914 (2000-07-25)
Several unnatural, predominantly hydrophobic nucleobases that pack efficiently in duplex DNA without hydrogen bonding functionalities are reported to circumvent the hydrogen bonding-based specificity, both during oligonucleotide hybridization and enzymatic DNA synthesis. The reported nucleoside analogs are efficient 'universal bases' for
E Naimi et al.
Nucleosides, nucleotides & nucleic acids, 20(8), 1533-1553 (2001-09-14)
A group of unnatural 1-(2-deoxy-beta-D-ribofuranosyl)isocarbostyrils having a variety of C-7 substituents [H, 4,7-(NO2)2, I, CF3, CN, (E)-CH=CH-I, -C triple bond CH, -C triple bond C-I, -C triple bond C-Br, -C=C-Me], designed as nucleoside mimics, were synthesized for evaluation as anticancer
Global Trade Item Number
| SKU | GTIN |
|---|---|
| CDS005198-100MG | 04061828956678 |
| 152102-5G | 04061833371633 |
| 152102-1G | 04061826661505 |
| 152102-10G | 04061833431481 |