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152102

Sigma-Aldrich

Isocarbostyril

98%

Synonym(s):

1(2H)-Isoquinolinone, 1-Hydroxyisoquinoline, 1-Isoquinolinol

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About This Item

Empirical Formula (Hill Notation):
C9H7NO
CAS Number:
491-30-5
Molecular Weight:
145.16
Beilstein:
2954
EC Number:
207-732-1
MDL number:
MFCD00006899
UNSPSC Code:
12352100
PubChem Substance ID:
24849199
NACRES:
NA.22

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

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Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Usman Ali et al.
Carbohydrate polymers, 209, 338-349 (2019-02-09)
The effect of wheat straw arabinoxylan (AX) and β-glucan stearic acid ester (SABG) composite coating on the quality and storage life of apple (Royal Delicious) was studied at 22 °C (±2) with relative humidity of 65% and 85% for 60 days.
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
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
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The incidences of diabetic mellitus and other metabolic diseases such as hypertension and hyperlipidemia are increasing worldwide; however, the current treatment is not able to control the rapidly increasing trend in diabetes mortality and morbidity. Studies related to the effectiveness
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