152102
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:
Molecular Weight:
145.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
207-732-1
Beilstein/REAXYS Number:
2954
MDL number:
Product Name
Isocarbostyril, 98%
InChI key
VDBNYAPERZTOOF-UHFFFAOYSA-N
InChI
1S/C9H7NO/c11-9-8-4-2-1-3-7(8)5-6-10-9/h1-6H,(H,10,11)
SMILES string
Oc1nccc2ccccc12.O=C3NC=Cc4ccccc34
assay
98%
form
solid
mp
211-214 °C (lit.)
Quality Level
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Related Categories
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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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
N K Richards et al.
Canadian journal of microbiology, 40(7), 561-566 (1994-07-01)
To facilitate the cloning of DNA encoding isoquinoline degradation an assay was developed that allowed the rapid visual scoring of the isoquinoline degradation phenotype of single colonies. Transposon mutagenesis of one of the isolates. Comamonas acidovorans IQ3, was performed using
R Erra-Balsells et al.
Carbohydrate research, 329(1), 157-167 (2000-11-22)
Matrix-assisted ultraviolet laser-desorption ionization time-of-flight mass spectrometry (UV-MALDI-TOF-MS) was applied to sulfated xylo-mannan fractions from Nothogenia fastigiata in order to determine their molecular weights and distribution profiles. The number-average molecular weight calculated from the spectra was similar to that determined
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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