2-Thiazolecarboxaldehyde

Modify Date: 2024-01-02 21:56:53

2-Thiazolecarboxaldehyde Structure
2-Thiazolecarboxaldehyde structure
Common Name 2-Thiazolecarboxaldehyde
CAS Number 10200-59-6 Molecular Weight 113.138
Density 1.4±0.1 g/cm3 Boiling Point 218.3±23.0 °C at 760 mmHg
Molecular Formula C4H3NOS Melting Point N/A
MSDS Chinese USA Flash Point 85.8±22.6 °C

 Names

Name 2-Thiazolecarboxaldehyde
Synonym More Synonyms

 Chemical & Physical Properties

Density 1.4±0.1 g/cm3
Boiling Point 218.3±23.0 °C at 760 mmHg
Molecular Formula C4H3NOS
Molecular Weight 113.138
Flash Point 85.8±22.6 °C
Exact Mass 112.993530
PSA 58.20000
LogP 0.50
Vapour Pressure 0.2±0.4 mmHg at 25°C
Index of Refraction 1.621
Storage condition Refrigerator (+4°C)
Water Solubility soluble

 Safety Information

Hazard Codes Xn:Harmful;
Risk Phrases R22;R36/37/38
Safety Phrases S36/37/39-S26-S23
WGK Germany 3
HS Code 2934100090

 Synthetic Route

 Customs

HS Code 2934100090
Summary 2934100090 other compounds containing an unfused thiazole ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

 Articles6

More Articles
Design, synthesis, antinociceptive and anti-inflammatory activities of novel piroxicam analogues.

Molecules 17(12) , 14126-45, (2012)

In this paper we report the design, synthesis, antinociceptive and anti-inflammatory activities of a series of benzothiazine N-acylhydrazones 14a–h, planned by structural modification of piroxicam (1)...

Asymmetric synthesis of an N-acylpyrrolidine for inhibition of HCV polymerase.

J. Org. Chem. 73(8) , 3094-102, (2008)

A practical asymmetric synthesis of a highly substituted N-acylpyrrolidine on multi-kilogram scale is described. The key step in the construction of the three stereocenters is a [3+2] cycloaddition of...

New highly active taxoids from 9 beta-dihydrobaccatin-9,10-acetals. Part 5.

Bioorg. Med. Chem. Lett. 14(12) , 3209-3215, (2004)

To improve the metabolic stability of 3, which exhibited both in vitro antitumor activity and in vivo efficacy by both iv and po administration, we designed and synthesized new taxane analogues. Most ...

 Synonyms

2-Thiazolecarboxaldehyde
MFCD00142924
Thiazole-2-carbaldehyde
1,3-Thiazole-2-carbaldehyde
2-Formylthiazole
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