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Merck
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文件

M31104

Sigma-Aldrich

α-甲基苄胺

99%

别名:

(±)-α-甲基苄胺, (±)-1-苯乙胺

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About This Item

线性分子式:
C6H5CH(CH3)NH2
CAS号:
618-36-0
分子量:
121.18
Beilstein:
636127
EC號碼:
210-545-8
MDL號碼:
MFCD00008069
分類程式碼代碼:
12352100
PubChem物質ID:
24896793
NACRES:
NA.22

化驗

99%

形狀

liquid

折射率

n20/D 1.526 (lit.)

bp

185 °C/756 mmHg (lit.)

密度

0.94 g/mL at 25 °C (lit.)

SMILES 字串

CC(N)c1ccccc1

InChI

1S/C8H11N/c1-7(9)8-5-3-2-4-6-8/h2-7H,9H2,1H3

InChI 密鑰

RQEUFEKYXDPUSK-UHFFFAOYSA-N

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相关类别

一般說明

α-甲基苄胺是一种氮源，被广泛用作研究伯胺化学酶动力学拆分的一种代表性底物。

應用

α-甲基苄胺可通过与外消旋双酚衍生物进行反应，用作合成二氢-5H-二苯并[c，e]氮杂环丙烷盐的反应物。
它可用于合成 o-氟苄胺。

象形圖

CorrosionExclamation mark
GHS05,GHS07

訊號詞

Danger

危險聲明

H302 + H312,H314

危險分類

Acute Tox. 4 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

儲存類別代碼

8A - Combustible corrosive hazardous materials

水污染物質分類（WGK）

WGK 1

閃點（°F）

158.0 °F - closed cup

閃點（°C）

70 °C - closed cup

個人防護裝備

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

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Whole-cell biocatalysis based on metabolically active baker's yeast with engineered transamination activity can be used to generate molecules carrying a chiral amine moiety. A prerequisite is though to express efficient ω-transaminases and to reach sufficient intracellular precursor levels. Herein, the
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Jan Dines Knudsen et al.
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Saccharomyces cerevisiae can be engineered to perform a multitude of different chemical reactions that are not programmed in its original genetic code. It has a large potential to function as whole-cell biocatalyst for one-pot multistep synthesis of various organic molecules
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