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Merck

83275

Sigma-Aldrich

4-吡咯烷基吡啶

purum, ≥98.0% (NT)

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About This Item

经验公式(希尔记法):
C9H12N2
CAS号:
分子量:
148.20
Beilstein:
472443
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

等級

purum

品質等級

化驗

≥98.0% (NT)

形狀

crystals

mp

54-58 °C (lit.)
55-61 °C

溶解度

methanol: 0.1 g/mL, clear

SMILES 字串

C1CCN(C1)c2ccncc2

InChI

1S/C9H12N2/c1-2-8-11(7-1)9-3-5-10-6-4-9/h3-6H,1-2,7-8H2

InChI 密鑰

RGUKYNXWOWSRET-UHFFFAOYSA-N

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其他說明

超强亲核酰化反应催化剂。综述

象形圖

Skull and crossbonesCorrosion

訊號詞

Danger

危險聲明

危險分類

Acute Tox. 3 Oral - Skin Corr. 1B

儲存類別代碼

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

水污染物質分類(WGK)

WGK 3

閃點(°F)

233.6 °F - closed cup

閃點(°C)

112 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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分析证书(COA)

Lot/Batch Number

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访问文档库

E.F. Scriven
Chemical Society Reviews, 12, 129-129 (1983)
A. Hassner
Tetrahedron, 34, 2069-2069 (1978)
Brian L Hodous et al.
Journal of the American Chemical Society, 124(34), 10006-10007 (2002-08-22)
The first method for the catalytic enantioselective addition of amines (specifically, pyrroles) to ketenes has been developed, and it has been demonstrated that the resulting acylpyrroles can be transformed into a broad spectrum of useful derivatives. On the basis of
H Kai et al.
The Journal of pharmacy and pharmacology, 48(1), 53-56 (1996-01-01)
We have examined the effects of pyridine derivatives on phosphatidylcholine secretion in primary cultures of rat type II pneumocytes. Of 12 pyridine derivatives, 4-aminopyridine, 4-dimethylaminopyridine and 4-pyrolidinopyridine had a stimulatory effect on phosphatidylcholine secretion, whereas other derivatives had little effect.
A method for the synthesis of isomerically pure saturated mixed-chain phosphatidylcholines.
J T Mason et al.
Analytical biochemistry, 113(1), 96-101 (1981-05-01)

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