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Merck
CN

552313

Sigma-Aldrich

4-苯基苄胺

97%

别名:

(4-Phenylphenyl)methanamine, 1-(Biphenyl-4-yl)methanamine, 4-(Aminomethyl)biphenyl, 4-Biphenylmethylamine, Biphenyl-4-ylmethanamine, [(1,1′-Biphenyl-4-yl)methyl]amine, [(Biphenyl-4-yl)methyl]amine, [1,1′-Biphenyl]-4-ylmethanamine, p-Phenylbenzylamine

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About This Item

线性分子式:
C6H5C6H4CH2NH2
CAS号:
分子量:
183.25
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

97%

mp

48-53 °C (lit.)

官能团

amine
phenyl

SMILES字符串

NCc1ccc(cc1)-c2ccccc2

InChI

1S/C13H13N/c14-10-11-6-8-13(9-7-11)12-4-2-1-3-5-12/h1-9H,10,14H2

InChI key

RMSPOVPGDBDYKH-UHFFFAOYSA-N

应用

4-Phenylbenzylamine may be used in the synthesis of:
  • squaric acid asymmetric diamides of glycopeptide antibiotics
  • asymmetric diamides of daunomycin and carminomycin
  • N-(biphenyl-4-ylmethyl)-1-hydroxy-6-thioxo-1,6-dihydropyridine-2-carboxamide

4-Phenylbenzylamine may also be used in the synthesis of Gd3+ chelates of DOTA(1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetate) type ligands.

其他说明

在氮气下处理和储存,以抑制杂质的形成。

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

224.6 °F - closed cup

闪点(°C)

107 °C - closed cup

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


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分析证书(COA)

Lot/Batch Number

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访问文档库

A new series of glycopeptide antibiotics incorporating a squaric acid moiety.
Sztaricskai F, et al.
The Journal of Antibiotics, 59(9), 564-564 (2006)
A new class of semisynthetic anthracycline glycoside antibiotics incorporating a squaric acid moiety.
Sztaricskai F, et al.
The Journal of Antibiotics, 58(11), 704-704 (2005)
chemical society(Great Britain)
Journal of the Chemical Society, Part 1 (1993)
Coupling fast water exchange to slow molecular tumbling in Gd3+ chelates: why faster is not always better.
Avedano S, et al.
Inorganic Chemistry, 52(15), 8436-8450 (2013)
Thioamide hydroxypyrothiones supersede amide hydroxypyrothiones in potency against anthrax lethal factor.
Agrawal A, et al.
Journal of Medicinal Chemistry, 52(4), 1063-1074 (2009)

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