Merck
CN

C4261

Sigma-Aldrich

香豆素

≥99% (HPLC)

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别名:
1,2-苯并吡喃酮, 1-苯并吡喃-2-酮, 2H-苯并吡喃-2-酮
Empirical Formula (Hill Notation):
C9H6O2
CAS号:
分子量:
146.14
Beilstein:
383644
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.25

蒸汽压

0.01 mmHg ( 47 °C)

质量水平

检测方案

≥99% (HPLC)

形式

powder

bp

298 °C (lit.)

mp

68-73 °C (lit.)

SMILES string

O=C1Oc2ccccc2C=C1

InChI

1S/C9H6O2/c10-9-6-5-7-3-1-2-4-8(7)11-9/h1-6H

InChI key

ZYGHJZDHTFUPRJ-UHFFFAOYSA-N

Gene Information

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此商品
72609PHL80017Y0000438
Coumarin ≥99% (HPLC)

Sigma-Aldrich

C4261

香豆素

Coumarin certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

Supelco

72609

香豆素

Coumarin phyproof® Reference Substance

PHL80017

香豆素

Coumarin European Pharmacopoeia (EP) Reference Standard

Y0000438

香豆素

bp

298 °C (lit.)

bp

298 °C (lit.)

bp

298 °C (lit.)

bp

298 °C (lit.)

mp

68-73 °C (lit.)

mp

68-73 °C (lit.)

mp

68-73 °C (lit.)

mp

68-73 °C (lit.)

vapor pressure

0.01 mmHg ( 47 °C)

vapor pressure

0.01 mmHg ( 47 °C)

vapor pressure

0.01 mmHg ( 47 °C)

vapor pressure

0.01 mmHg ( 47 °C)

form

powder

form

-

form

flakes

form

-

Gene Information

rat ... Maoa(29253), Maob(25750)

Gene Information

-

Gene Information

-

Gene Information

-

应用

香豆素可用作制备或合成基于香豆素的抗凝血剂、抗炎剂和抗氧化剂超氧化物清除剂的前体分子。

象形图

Skull and crossbones

警示用语:

Danger

危险声明

危险分类

Acute Tox. 3 Dermal - Acute Tox. 3 Oral - Skin Sens. 1

储存分类代码

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 1

闪点(°F)

323.6 °F - closed cup

闪点(°C)

162 °C - closed cup

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Donglei Yu et al.
Medicinal research reviews, 23(3), 322-345 (2003-03-21)
Numerous plant-derived compounds have been evaluated for inhibitory effects against HIV replication, and some coumarins have been found to inhibit different stages in the HIV replication cycle. This review article describes recent progress in the discovery, structure modification, and structure-activity
Shigehiro Sumiya et al.
The journal of physical chemistry. A, 117(7), 1474-1482 (2013-01-25)
A coumarin-amide-dipicolylamine linkage (L) was synthesized and used as a fluorescent receptor for metal cations in water. The receptor dissolved in water with neutral pH shows almost no fluorescence due to the photoinduced electron transfer (PET) from the amide and
Shota Morimoto et al.
Chemical communications (Cambridge, England), 49(18), 1811-1813 (2013-01-26)
A photo-switchable fluorescent flagging approach has been developed to identify photoaffinity-labeled peptides in target protein. Upon photochemical release of the ligand, the protein was newly modified with a coumarin in place of the previously attached biotin. It allowed us to
A Marjolein Schrijver et al.
Journal of endovascular therapy : an official journal of the International Society of Endovascular Specialists, 22(1), 87-95 (2015-03-17)
To report the results of the Dutch randomized trial comparing standard catheter-directed and ultrasound-accelerated thrombolysis (UST) for the treatment of arterial thromboembolic occlusions. The DUET study ( controlled-trials.com ; identifier ISRCTN72676102) was designed to assess whether UST can reduce therapy
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Clinical pharmacology and therapeutics, 92(6), 746-756 (2012-11-08)
A systematic review and a meta-analysis were performed to quantify the accumulated information from genetic association studies investigating the impact of the CYP4F2 rs2108622 (p.V433M) polymorphism on coumarin dose requirement. An additional aim was to explore the contribution of the

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