推荐产品
方案
98%
mp
34-37 °C (lit.)
官能团
aldehyde
chloro
储存温度
2-8°C
SMILES字符串
Clc1ccc(C=O)o1
InChI
1S/C5H3ClO2/c6-5-2-1-4(3-7)8-5/h1-3H
InChI key
DGAUAVDWXYXXGQ-UHFFFAOYSA-N
一般描述
5-Chloro-2-furaldehyde is also known as 5-chlorofurfural. It reacts with aniline and aniline hydrochloride to form bis-(phenylamino) derivatives, without the furan ring cleavage. It also undergoes coupling with ethyl acetoacetate to form the corresponding ethyl bis-acetoacetate.
应用
5-Chloro-2-furaldehyde may be used as an internal standard during the analysis of furanic compounds by reversed-phase-high performance liquid chromatography–diode array detection (RP-HPLC–DAD) method.
警示用语:
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
The Synthesis of Substituted ?-Thienyl-and ?-Furylglutaric Acids.
Journal of the American Chemical Society, 76(10), 2731-2732 (1954)
Waterpipe smoke: a considerable source of human exposure against furanic compounds.
Analytica Chimica Acta, 709, 105-112 (2012)
Utilization of potassium vinyltrifluoroborate in the development of a 1, 2-dianion equivalent.
Organic Letters, 11(11), 2369-2372 (2009)
The Reaction of Certain Substituted Furfurals with Aniline and Aniline Hydrochloride.
Journal of the American Chemical Society, 74(10), 2626-2628 (1952)
?-Selective directed catalytic asymmetric hydroboration of 1,1-disubstituted alkenes.
Chemical Communications (Cambridge, England), 48(100), 12180-12182 (2012)
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