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72609

Supelco

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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About This Item

经验公式（希尔记法）:
C9H6O2
CAS号:
91-64-5
分子量:
146.14
Beilstein:
383644
EC號碼:
202-086-7
MDL號碼:
MFCD00006850
分類程式碼代碼:
41116107
PubChem物質ID:
329764209
NACRES:
NA.24

等級

certified reference material
TraceCERT®

品質等級

300

蒸汽壓力

0.01 mmHg ( 47 °C)

儲存期限

limited shelf life, expiry date on the label

製造商／商標名

Manufactured by: Sigma-Aldrich Production GmbH, Switzerland

技術

HPLC: suitable
gas chromatography (GC): suitable

bp

298 °C (lit.)

mp

68-73 °C (lit.)

應用

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

形式

neat

SMILES 字串

O=C1Oc2ccccc2C=C1

InChI

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

InChI 密鑰

ZYGHJZDHTFUPRJ-UHFFFAOYSA-N

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相关类别

一般說明

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。

應用

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。

包裝

无底玻璃瓶。内含物装在插入的融合锥内。

其他說明

This compound is commonly found in plants of the genus: cinnamomum curcuma hedera humulus melissa mentha salvia sambucus zingiber

法律資訊

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

象形圖

Skull and crossbones
GHS06

訊號詞

Danger

危險聲明

H301 + H311,H317

危險分類

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

儲存類別代碼

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

水污染物質分類（WGK）

WGK 1

閃點（°F）

323.6 °F - closed cup

閃點（°C）

162 °C - closed cup

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分析证书(COA)

Lot/Batch Number
BCCK3254
BCCB9573
BCBR7238V

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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
Klaus Abraham et al.
Molecular nutrition & food research, 54(2), 228-239 (2009-12-22)
Coumarin is a secondary phytochemical with hepatotoxic and carcinogenic properties. For the carcinogenic effect, a genotoxic mechanism was considered possible, but was discounted by the European Food Safety Authority in 2004 based on new evidence. This allowed the derivation of
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)
Kamilia M Amin et al.
European journal of medicinal chemistry, 60, 187-198 (2013-01-08)
Two groups of coumarin-pyrazoline hybrids were synthesized. The target compounds were obtained by cyclization of the coumarin chalcones with various substituted hydrazines to produce the corresponding pyrazolines through 1,4-addition on α,β-unsaturated carbonyl system. Selected compounds were investigated for their anticancer
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)
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