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安全信息

704938

Sigma-Aldrich

N-苄基-2-溴-N-苯基丙酰胺

97%

别名:

2-溴-N-苯基-N-(苯基甲基)丙酰胺, N-苄基-2-溴-丙酰苯胺

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About This Item

经验公式（希尔记法）:
C16H16BrNO
CAS号:
93010-41-4
分子量:
318.21
MDL编号:
MFCD12406811
UNSPSC代码:
12352100
PubChem化学物质编号:
329762492
NACRES:
NA.22

方案

97%

表单

solid

mp

75-80 °C

官能团

amide
bromo
phenyl

SMILES字符串

CC(Br)C(=O)N(Cc1ccccc1)c2ccccc2

InChI

1S/C16H16BrNO/c1-13(17)16(19)18(15-10-6-3-7-11-15)12-14-8-4-2-5-9-14/h2-11,13H,12H2,1H3

InChI key

SVPMVGLFGUEUOK-UHFFFAOYSA-N

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Anti-ACTL7B antibody produced in mouse

Monoclonal Anti-ACTB antibody produced in mouse clone 3G4-F9, purified immunoglobulin, buffered aqueous solution

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Monoclonal Anti-ACTB antibody produced in mouse

Monoclonal Anti-ACTL6A antibody produced in mouse clone 3E4, purified immunoglobulin, buffered aqueous solution

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Monoclonal Anti-ACTL6A antibody produced in mouse

clone

6A4, monoclonal

clone

polyclonal

clone

3G4-F9, monoclonal

clone

3E4, monoclonal

species reactivity

human

species reactivity

human

species reactivity

human, rat, mouse

species reactivity

human

antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

biological source

mouse

biological source

mouse

biological source

mouse

biological source

mouse

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

应用

用于双唑啉型吡啶-镍络合物催化的不对称根岸偶联反应。[1]

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险分类

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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    Lot/Batch Number
    07296TJ

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    Christian Fischer et al.
    Journal of the American Chemical Society, 127(13), 4594-4595 (2005-03-31)
    A Ni/Pybox catalyst achieves the asymmetric cross-coupling of secondary alpha-bromo amides with organozinc reagents. The process tolerates a variety of functional groups and affords the desired product in good yield and in high enantiomeric excess.

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