すべての画像(3)
About This Item
実験式（ヒル表記法）:
C7H5N
CAS番号:
分子量:
103.12
MDL番号:
UNSPSCコード:
12352100
PubChem Substance ID:
NACRES:
NA.22
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品質水準
アッセイ
98%
bp
83-84 °C/30 mmHg (lit.)
mp
39-40 °C (lit.)
SMILES記法
C#Cc1cccnc1
InChI
1S/C7H5N/c1-2-7-4-3-5-8-6-7/h1,3-6H
InChI Key
CLRPXACRDTXENY-UHFFFAOYSA-N
シグナルワード
Danger
危険有害性情報
危険有害性の分類
Eye Irrit. 2 - Flam. Sol. 1 - Skin Irrit. 2 - STOT SE 3
ターゲットの組織
Respiratory system
保管分類コード
4.1B - Flammable solid hazardous materials
WGK
WGK 3
引火点(°F)
134.0 °F - closed cup
引火点(℃)
56.67 °C - closed cup
個人用保護具 (PPE)
dust mask type N95 (US), Eyeshields, Gloves
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
消防法
第4類:引火性液体
第二石油類
危険等級III
非水溶性液体
Jan Code
520446-VAR:
520446-5G:
520446-BULK:
520446-1G:
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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
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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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