assay
97%
refractive index
n20/D 1.604 (lit.)
bp
99 °C/21 mmHg (lit.)
density
1.376 g/mL at 25 °C (lit.)
functional group
aldehyde, chloro
SMILES string
[H]C(=O)c1ccc(Cl)s1
InChI
1S/C5H3ClOS/c6-5-2-1-4(3-7)8-5/h1-3H
InChI key
VWYFITBWBRVBSW-UHFFFAOYSA-N
General description
5-Chloro-2-thiophenecarboxaldehyde is a thiophene derivative.
Application
5-Chloro-2-thiophenecarboxaldehyde may be used for synthesis of 2-heteroaryl-α-methyl-5-benzoxazoleacetic acids and N,N′-bis[(E)-(5-chloro-2-thienyl)methylidene]ethane-1,2-diamine
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral
存储类别
10 - Combustible liquids
wgk
WGK 3
flash_point_f
208.4 °F - closed cup
flash_point_c
98 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
新产品
此项目有
M da Consolação et al.
Journal of medicinal chemistry, 18(11), 1159-1161 (1975-11-01)
Lapachol [2-hydroxy-3-(3-methyl-2-butenyl)-1,4-naphthoquinone] and its analogs [2-(3,7-dimethyl-2,6-octadienyl)-3-hydroxy-1,4-naphthoquinone and 2-(3,3-dibromo-2-propenyl)-3-hydroxy-1,4-naphthoquinone] have been described, among almost a hundred synthesized analogs, as active against rat tumor Walker 256 carcinosarcoma. The acetylglucosylation of lapachol results in a compound which extends lapachol activity becoming effective against
N, N'-Bis [(E)-(5-chloro-2-thienyl) methylidene] ethane-1, 2-diamine.
Prasath R, et al.
Acta Crystallographica Section E, Structure Reports Online, 66(11), o2883-o2883 (2010)
Synthesis of 6-(Thienylmethylene)penam Sulfones and their ?-Lactamase Inhibitory Activities.
Kim DH, et al.
Yakhak Hoechi, 51(6) (2007)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 443239-5G | 04061837614934 |
| 443239-1G | 04061832282923 |