5-Chloro-2-thiophenecarbaldehyde

Names

[ Name ]:
5-Chloro-2-thiophenecarbaldehyde

[Synonym ]:
EINECS 230-708-7
5-Chloro-2-thiophenecarboxaldehyde
5-Chloro-2-thiophenecarbaldehyde
2-Thiophenecarboxaldehyde, 5-chloro-
5-chlorothiophene-2-carbaldehyde
MFCD00047090

Biological Activity

[Description]:

2-Chloro-5-thiophenecarboxaldehyde is a biochemical reagent that can be used as a biological material or organic compound for life science related research.

[Related Catalog]:

Research Areas >> Others

Signaling Pathways >> Others >> Others

Chemical & Physical Properties

[ Density]:
1.4±0.1 g/cm3

[ Boiling Point ]:
221.1±20.0 °C at 760 mmHg

[ Molecular Formula ]:
C₅H₃ClOS

[ Molecular Weight ]:
146.59

[ Flash Point ]:
87.5±21.8 °C

[ Exact Mass ]:
145.959305

[ PSA ]:
45.31000

[ LogP ]:
1.68

[ Vapour Pressure ]:
0.1±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.626

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H302-H312-H332

[ Precautionary Statements ]:
P280

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xn: Harmful;

[ Risk Phrases ]:
R20/21/22

[ Safety Phrases ]:
S36-S36/37/39-S26-S24

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ HS Code ]:
2934999090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2934999090

[ Summary ]:
2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

A lapachol derivative active against mouse lymphocytic leukemia P-388.

J. Med. Chem. 18(11) , 1159-61, (1975)

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...

Synthesis and antiinflammatory activity of some 2-heteroaryl-alpha-methyl-5-benzoxazoleacetic acids.

J. Med. Chem. 18(11) , 1158-9, (1975)

The syntheses of eight of the title compounds are described. The compounds possessed activity comparable with that of the previously tested 2-substituted phenyl analogs in the carrageenan-induced rat ...

N, N'-Bis [(E)-(5-chloro-2-thienyl) methylidene] ethane-1, 2-diamine. Prasath R, et al.

Acta Crystallogr. Sect. E Struct. Rep. Online 66(11) , o2883, (2010)