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Merck

201014

Sigma-Aldrich

N-苄基苯甲酰胺

≥98%

别名:

Benzoic acid benzylamide, N-(Phenylmethyl)benzamide, N-Benzoylbenzylamine

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About This Item

线性分子式:
C6H5CONHCH2C6H5
CAS号:
分子量:
211.26
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:

品質等級

化驗

≥98%

mp

104-106 °C (lit.)

溶解度

acetone: 25 mg/mL, clear, colorless

SMILES 字串

O=C(NCc1ccccc1)c2ccccc2

InChI

1S/C14H13NO/c16-14(13-9-5-2-6-10-13)15-11-12-7-3-1-4-8-12/h1-10H,11H2,(H,15,16)

InChI 密鑰

LKQUCICFTHBFAL-UHFFFAOYSA-N

一般說明

N-苄基苯甲酰胺抑制酪氨酸酶的活性

應用

α 取代苄胺的便捷前体,用于滴定丁基锂和其他锂碱的指示剂。相关参考文献,请参见 Aldrichimica Acta

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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Aldrichimica Acta, 11, 20-20 (1978)
Yae Eun Chong et al.
Biomedical chromatography : BMC, 33(11), e4653-e4653 (2019-07-20)
Ondansetron, a widely used antiemetic agent, is a P-glycoprotein (P-gp) substrate and therefore expression of P-gp at the blood-brain barrier limits its distribution to the central nervous system (CNS), which was observed to be reversed by coadministration with P-gp inhibitors.
Zsanett Dorkó et al.
Talanta, 162, 167-173 (2016-11-14)
A simple and efficient method is presented for assessing molecularly imprinted polymers (MIP) and other sorbents from the point of view of practical applications. The adsorption isotherms of the compounds, which need to be separated or detected in an application
Sung Jin Cho et al.
Bioorganic & medicinal chemistry letters, 16(10), 2682-2684 (2006-03-04)
A series of potent inhibitors of tyrosinase and their structure-activity relationships are described. N-Benzylbenzamide derivatives (1-21) with hydroxyl(s) were synthesized and tested for their tyrosinase inhibitory activity. With this series, compound 15 provided a potent tyrosinase inhibition: it effectively inhibited

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