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3-乙炔基吡啶

3-乙炔基吡啶用途

3-乙炔基吡啶是一种生物化学试剂,可作为生物材料或有机化合物进行生命科学相关研究。

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3-乙炔基吡啶名称

[ CAS 号 ]:
2510-23-8

[ 中文名 ]:
3-乙炔基吡啶

[ 英文名 ]:
3-Ethynylpyridine

[中文别名 ]:

[英文别名 ]:

pyridine,3-ethynyl
meta-ethynylpyridine
MFCD02177459
3-pyridylacetylene
3-pyridinyl acetylene
3-Ethynylpyridine
Pyridine, 3-ethynyl-
3-ethynyl pyridine

3-乙炔基吡啶生物活性

[ 描述 ]:

3-乙炔基吡啶是一种生物化学试剂,可作为生物材料或有机化合物进行生命科学相关研究。

[ 相关类别 ]:

研究领域 >> 其他

信号通路 >> 其他 >> 其他

3-乙炔基吡啶物理化学性质

[ 密度 ]:
1.0±0.1 g/cm3

[ 沸点 ]:
170.5±13.0 °C at 760 mmHg

[ 熔点 ]:
39-40 °C(lit.)

[ 分子式 ]:
C₇H₅N

[ 分子量 ]:
103.12

[ 闪点 ]:
57.5±12.4 °C

[ 精确质量 ]:
103.042198

[ PSA ]:
12.89000

[ LogP ]:
0.91

[ 外观性状 ]:
固体;White to Gray to Brown powder to crystal

[ 蒸汽压 ]:
1.9±0.3 mmHg at 25°C

[ 折射率 ]:
1.543

[ 储存条件 ]:
Freezer

3-乙炔基吡啶MSDS

3-乙炔基吡啶安全信息

[ 符号 ]:

GHS02, GHS07

[ 信号词 ]:
Danger

[ 危害声明 ]:
H228-H315-H319-H335

[ 警示性声明 ]:
P210-P261-P305 + P351 + P338

[ 个人防护装备 ]:
dust mask type N95 (US);Eyeshields;Gloves

[ 危害码 (欧洲) ]:
Xi: Irritant;F: Flammable;

[ 风险声明 (欧洲) ]:
R36/37/38

[ 安全声明 (欧洲) ]:
S16-S26-S36

[ 危险品运输编码 ]:
UN 1325 4.1/PG 2

[ WGK德国 ]:
3

[ 危险类别 ]:
4.1

[ 海关编码 ]:
2933399090

3-乙炔基吡啶合成路线

3-乙炔基吡啶海关

[ 海关编码 ]: 2933399090

[ 中文概述 ]:
2933399090. 其他结构含非稠合吡啶环的化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%

[ 申报要素 ]: 品名, 成分含量, 用途, 乌洛托品请注明外观, 6－己内酰胺请注明外观, 签约日期

[ Summary ]:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

3-乙炔基吡啶文献

Sequential one-pot ruthenium-catalyzed azide-alkyne cycloaddition from primary alkyl halides and sodium azide.

J. Org. Chem. 76(7) , 2355-9, (2011)

An experimentally simple sequential one-pot RuAAC reaction, affording 1,5-disubstituted 1H-1,2,3-triazoles in good to excellent yields starting from an alkyl halide, sodium azide, and an alkyne, is re...

Homochiral supramolecular M2L4 cages by high-fidelity self-sorting of chiral ligands.

Chemistry 19(33) , 10890-4, (2013)

A 1,1'-binaphthyl-based bis(pyridine) ligand (1) was prepared in racemic and enantiomerically pure form to study the formation of [Pd2(1)4] complexes upon coordination to palladium(II) ions with regar...

Direct use of dioxygen as an oxygen source: catalytic oxidative synthesis of amides.

Chem. Commun. (Camb.) 48(2) , 305-7, (2012)

The first transition-metal-catalyzed direct oxidative synthesis of amides by using dioxygen as an oxygen source has been developed under mild conditions, in which DBU was used as the key additive. The...

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