Merck
CN

358991

Sigma-Aldrich

N-叔丁基甲胺

97%

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别名:
N-甲基-叔丁胺
线性分子式:
(CH3)3CNHCH3
CAS号:
分子量:
87.16
Beilstein:
1730941
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

97%

形式

liquid

折射率

n20/D 1.395 (lit.)

bp

67-69 °C (lit.)

密度

0.727 g/mL at 25 °C (lit.)

SMILES string

CNC(C)(C)C

InChI

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

InChI key

ZQGJEUVBUVKZKS-UHFFFAOYSA-N

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34490471232455709
N-tert-Butylmethylamine 97%

Sigma-Aldrich

358991

N-叔丁基甲胺

Dibutylamine puriss., ≥99.0% (GC)

Sigma-Aldrich

34490

二丁胺

Dibutylamine ≥99.5%

Sigma-Aldrich

471232

二丁胺

N-tert-Butyldiethanolamine 97%

Sigma-Aldrich

455709

N-叔丁基二乙醇胺

form

liquid

form

-

form

liquid

form

solid

refractive index

n20/D 1.395 (lit.)

refractive index

n20/D 1.417 (lit.)

refractive index

n20/D 1.417 (lit.)

refractive index

n20/D 1.4666 (lit.)

bp

67-69 °C (lit.)

bp

159 °C (lit.)

bp

159 °C (lit.)

bp

136-139 °C/12 mmHg (lit.)

density

0.727 g/mL at 25 °C (lit.)

density

0.767 g/mL at 25 °C (lit.)

density

0.767 g/mL at 25 °C (lit.)

density

0.983 g/mL at 25 °C (lit.)

应用

N-tert-Butylmethylamine may be used in the preparation of 3-benzyl-N-tert-butyl-N,3-dimethyl-2,3-dihydrobenzofuran-6-carboxamide. N-tert-Butylmethylamine (N-Methyl-tert-butylamine) may be used in the preparation of 2-(α-N-methyl-tert-butylaminobenzyl)-1-indenone.

警示用语:

Danger

危险分类

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)

-14.8 °F - closed cup

闪点(°C)

-26 °C - closed cup

个人防护装备

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

法规信息

危险化学品

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Sigma-Aldrich

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十二烷基异氰酸酯

Mobile keto allyl systems. XVI. Thermal decomposition of 2-(. alpha.-N-methyl-tert-butylaminobenzyl)-1-indenone. Deamination-rearrangement.
Murray RJ and Cromwell NH.
The Journal of Organic Chemistry, 39(26), 3939-3941 (1974)
Philippe Diaz et al.
ChemMedChem, 4(10), 1615-1629 (2009-07-29)
We recently discovered and reported a series of N-alkyl-isatin acylhydrazone derivatives that are potent cannabinoid receptor 2 (CB(2)) agonists. In an effort to improve the druglike properties of these compounds and to better understand and improve the treatment of neuropathic
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The Journal of antibiotics, 69(11), 825-834 (2016-03-31)
A series of 20 xanthone derivatives was synthesized and evaluated for anti-Helicobacter pylori (H. pylori) activity. Qualitative and quantitative in vitro tests using the Kirby-Bauer method (agar disc-diffusion method) were performed. The tested compounds were screened against clarithromycin- and/or metronidazole-resistant

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