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Merck
CN

72609

香豆素

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

别名:

1,2-苯并吡喃酮, 1-苯并吡喃-2-酮, 2H-苯并吡喃-2-酮

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关于此项目

经验公式（希尔记法）:
C9H6O2
化学文摘社编号:
91-64-5
分子量:
146.14
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329764209
EC Number:
202-086-7
Beilstein/REAXYS Number:
383644
MDL number:
MFCD00006850

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产品名称

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

InChI key

ZYGHJZDHTFUPRJ-UHFFFAOYSA-N

InChI

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

SMILES string

O=C1Oc2ccccc2C=C1

grade

certified reference material
TraceCERT®

vapor pressure

0.01 mmHg ( 47 °C)

shelf life

limited shelf life, expiry date on the label

manufacturer/tradename

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

bp

298 °C (lit.)

mp

68-73 °C (lit.)

application(s)

cleaning products
cosmetics
environmental
flavors and fragrances
food and beverages
personal care

format

neat

Quality Level

300

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相关类别

Application

有关合适仪器技术的更多信息，请参考产品分析证书。如需进一步支持，请联系技术服务部门。

General description

该认证标准物质（CRM）根据ISO/IEC 17025和ISO 17034进行生产和认证。该CRM可追溯到来自NMI的原材料，如 NIST或NMIJ。
证书上给出了定量核磁共振法认证的内容，包括不确定性和失效日期。
请访问http://www.sigma-aldrich.com下载您的证书。

Other Notes

这种化合物常见于以下属的植物中：肉桂 姜黄 常春藤 香蜂草 薄荷 鼠尾草接骨木

Packaging

无底玻璃瓶。内含物装在插入的融合锥内。

Legal Information

TraceCERT is a registered trademark of Merck KGaA, Darmstadt, Germany

pictograms

Skull and crossbones
GHS06

signalword

Danger

Hazard Classifications

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

存储类别

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

wgk

WGK 1

flash_point_f

323.6 °F - closed cup

flash_point_c

162 °C - closed cup

分析证书(COA)

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Yutao Yang et al.
Biosensors & bioelectronics, 47, 300-306 (2013-04-17)
The synthesis and characterization of a coumarin-chromene (8, 9-dihydro-2H-cyclopenta[b]pyrano[2,3-f]chromene-2,10(7aH)-dione) (1) derivative and its use for thiol chemosensing in water was reported. Experimental details showed 1 acts as a probe for the detection of thiols including cysteine (Cys), homocysteine (Hcy) and
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
A ratiometric fluorescent probe for rapid detection of hydrogen sulfide in mitochondria.
Yuncong Chen et al.
Angewandte Chemie (International ed. in English), 52(6), 1688-1691 (2013-01-05)
Musiliyu A Musa et al.
Current medicinal chemistry, 15(26), 2664-2679 (2008-11-11)
The coumarin (benzopyran-2-one, or chromen-2-one) ring system, present in natural products (such as the anticoagulant warfarin) that display interesting pharmacological properties, has intrigued chemists and medicinal chemists for decades to explore the natural coumarins or synthetic analogs for their applicability
Sukhendu Maiti et al.
Journal of the American Chemical Society, 135(11), 4567-4572 (2013-03-07)
We present here, the design, synthesis, spectroscopic characterization, and in vitro biological assessment of a gemcitabine-coumarin-biotin conjugate (5). Probe 5 is a multifunctional molecule composed of a thiol-specific cleavable disulfide bond, a coumarin moiety as a fluorescent reporter, gemcitabine (GMC)
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