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Merck
CN

162124

Sigma-Aldrich

N-丁基甲胺

96%

别名:

N-甲基丁胺

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About This Item

线性分子式:
CH3NH(CH2)3CH3
CAS号:
分子量:
87.16
Beilstein:
1209231
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:

方案

96%

折射率

n20/D 1.3995 (lit.)

沸点

90.5-91.5 °C (lit.)

密度

0.736 g/mL at 25 °C (lit.)

SMILES字符串

CCCCNC

InChI

1S/C5H13N/c1-3-4-5-6-2/h6H,3-5H2,1-2H3

InChI key

QCOGKXLOEWLIDC-UHFFFAOYSA-N

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应用

N-Butylmethylamine was used in synthesis of N-n-butyl-N-methyl-N-2-(1-phenyl)propyl-amine and 16α-(bromoalkylamide) derivatives of estradiol.

警示用语:

Danger

危险分类

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Flam. Liq. 2 - Skin Corr. 1B

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

30.2 °F - closed cup

闪点(°C)

-1 °C - closed cup

个人防护装备

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

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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The availability of clean water from the already scarce sources is threatened by continuous addition of contaminated industrial and of abattoir waste into watercourses globally. The aim of the current study was to reduce the amount of waste produced, to
A Base-Catalyzed Domino-Isomerization-Hydroamination Reaction-A New Synthetic Route to Amphetamines.
Hartung CG, et al.
Tetrahedron, 56(29), 5157-5162 (2000)
J D Pelletier et al.
Bioorganic & medicinal chemistry, 4(10), 1617-1628 (1996-10-01)
To develop inhibitors of 17 beta-hydroxysteroid dehydrogenase (17 beta-HSD) without residual estrogenic activity, the synthesis of 16 alpha-(bromoalkylamide) derivatives of estradiol was performed starting from a key intermediate aldehyde obtained from commercially available estrone. In addition, series of 16 alpha-(bromoalkyl)

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