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Merck
모든 사진(3)

Key Documents

642673

Sigma-Aldrich

3-Hydroxycoumarin

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About This Item

실험식(Hill 표기법):
C9H6O3
CAS Number:
Molecular Weight:
162.14
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

형태

solid

mp

153-157 °C (lit.)

SMILES string

OC1=Cc2ccccc2OC1=O

InChI

1S/C9H6O3/c10-7-5-6-3-1-2-4-8(6)12-9(7)11/h1-5,10H

InChI key

MJKVTPMWOKAVMS-UHFFFAOYSA-N

픽토그램

Exclamation mark

신호어

Warning

유해 및 위험 성명서

예방조치 성명서

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable

개인 보호 장비

dust mask type N95 (US), Eyeshields, Gloves


시험 성적서(COA)

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Journal of fluorescence, 27(3), 895-919 (2017-02-22)
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Alberto Valdés et al.
Food research international (Ottawa, Ont.), 137, 109368-109368 (2020-11-26)
Several works have been focused on the extraction of polysaccharides, polyphenols and caffeine from spent coffee grounds (SCG) and their application in food formulations, but the peptide bioactivity from SCG protein hydrolysates has never been addressed. In the present work
Paweł Mateusz Nowak et al.
Journal of chromatography. A, 1548, 92-99 (2018-03-22)
The use of migration times and peak areas referred to another sample component - internal standard, brings many benefits in improving reliability of capillary electrophoresis. However, it is quite commonly overlooked that despite relative migration time and peak area ratio
T C Marques et al.
Reproduction in domestic animals = Zuchthygiene, 53(1), 226-236 (2017-12-06)
Effects of adding different concentrations of melatonin (10
Valeria Nori et al.
Beilstein journal of organic chemistry, 16, 1084-1091 (2020-06-20)
Cascade cyclocarbopalladation of the readily available aryl/alkyl-substituted propargylic amides containing an aryl iodide moiety, followed by Suzuki-Miyaura coupling with arylboronic acids, allowed an efficient regio- and stereoselective synthesis of tetrasubstituted 4-methylene-3,4-dihydroisoquinolin-1(2H)-ones. Moreover, cascade cyclocarbopalladation, followed by the reaction with 2-alkynyltrifluoroacetanilides

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