所有图片(3)
About This Item
经验公式（希尔记法）:
C7H5N
CAS号:
分子量:
103.12
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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质量水平
方案
98%
沸点
83-84 °C/30 mmHg (lit.)
mp
39-40 °C (lit.)
SMILES字符串
C#Cc1cccnc1
InChI
1S/C7H5N/c1-2-7-4-3-5-8-6-7/h1,3-6H
InChI key
CLRPXACRDTXENY-UHFFFAOYSA-N
警示用语：
Danger
危险分类
Eye Irrit. 2 - Flam. Sol. 1 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
4.1B - Flammable solid hazardous materials
WGK
WGK 3
闪点(°F)
134.0 °F - closed cup
闪点(°C)
56.67 °C - closed cup
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
Varinder K Aggarwal et al.
The Journal of organic chemistry, 68(13), 5381-5383 (2003-06-21)
A convenient one-pot procedure for the preparation of pyrazoles by 1,3-dipolar cycloaddition of diazo compounds generated in situ has been developed. Diazo compounds derived from aldehydes were reacted with terminal alkynes to furnish regioselectively 3,5-disubstituted pyrazoles. Furthermore, the reaction of
Christoph Gütz et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(33), 10890-10894 (2013-07-05)
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 regard to the degree of chiral self-sorting. The self-assembly process proceeds in a highly
Wei Wei et al.
Chemical communications (Cambridge, England), 48(2), 305-307 (2011-11-18)
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 present methodology, which utilizes dioxygen as an oxidant and
Qing Li et al.
Marine drugs, 16(4) (2018-03-31)
Chitosan is an abundant and renewable polysaccharide, which exhibits attractive bioactivities and natural properties. Improvement such as chemical modification of chitosan is often performed for its potential of providing high bioactivity and good water solubility. A new class of chitosan
Johan R Johansson et al.
The Journal of organic chemistry, 76(7), 2355-2359 (2011-03-11)
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 reported. The organic azide is formed in situ by treating the primary alkyl halide
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