All Photos(1)
About This Item
Empirical Formula (Hill Notation):
C5H3ClO2
CAS Number:
Molecular Weight:
130.53
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
![Benzo[b]thiophene-2-carboxaldehyde 97%](/deepweb/assets/sigmaaldrich/product/structures/321/060/32405a4e-5720-4c6d-91cf-115c747270c4/640/32405a4e-5720-4c6d-91cf-115c747270c4.png)
Assay
98%
mp
34-37 °C (lit.)
functional group
aldehyde
chloro
storage temp.
2-8°C
SMILES string
Clc1ccc(C=O)o1
InChI
1S/C5H3ClO2/c6-5-2-1-4(3-7)8-5/h1-3H
InChI key
DGAUAVDWXYXXGQ-UHFFFAOYSA-N
General description
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.
Application
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.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
The Reaction of Certain Substituted Furfurals with Aniline and Aniline Hydrochloride.
Drisko RW and McKennis Jr H.
Journal of the American Chemical Society, 74(10), 2626-2628 (1952)
?-Selective directed catalytic asymmetric hydroboration of 1,1-disubstituted alkenes.
Smith SM, et al.
Chemical Communications (Cambridge, England), 48(100), 12180-12182 (2012)
Waterpipe smoke: a considerable source of human exposure against furanic compounds.
Schubert J, et al.
Analytica Chimica Acta, 709, 105-112 (2012)
Utilization of potassium vinyltrifluoroborate in the development of a 1, 2-dianion equivalent.
Molander GA and Sandrock Deidre L
Organic Letters, 11(11), 2369-2372 (2009)
The Synthesis of Substituted ?-Thienyl-and ?-Furylglutaric Acids.
Smith Jr WT and Shelton RW.
Journal of the American Chemical Society, 76(10), 2731-2732 (1954)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service