ChemicalBook >> CAS DataBase List >>1,3-Thiazole-2-carbaldehyde

1,3-Thiazole-2-carbaldehyde

CAS No.
10200-59-6
Chemical Name:
1,3-Thiazole-2-carbaldehyde
Synonyms
THIAZOLE-2-CARBALDEHYDE;20:5n3);EOS-61959;2-FORMYLTHIAZOLE;2-Formylthiazole>2-Formyl-1,3-thiazole;2-Thiazolecarbaldehyde;thiazol-2-carbaldehyde;eicosapentaenoate (EPA;2-THIAZOLECARBOXALDEHYDE
CBNumber:
CB4493103
Molecular Formula:
C4H3NOS
Molecular Weight:
113.14
MDL Number:
MFCD00142924
MOL File:
10200-59-6.mol
MSDS File:
SDS
Last updated:2026-01-13 11:20:26
Product description Number Pack Size Price
2-Thiazolecarboxaldehyde 97% 422460 1g $81.79
2-Formylthiazole >97.0%(GC) F0303 1g $39
2-Formylthiazole >97.0%(GC) F0303 5g $127
2-Thiazolecarboxaldehyde 97% JK613181 1g $98
Thiazole-2-carboxaldehyde 98% 069072 25g $119
More product size

1,3-Thiazole-2-carbaldehyde Properties

Boiling point 61-63 °C/15 mmHg (lit.)
Density 1.288 g/mL at 25 °C (lit.)
refractive index n20/D 1.574(lit.)
Flash point 154 °F
storage temp. 2-8°C
pka 0.44±0.10(Predicted)
form Liquid
color Colorless to pale yellow
Water Solubility soluble
InChI InChI=1S/C4H3NOS/c6-3-4-5-1-2-7-4/h1-3H
InChIKey ZGTFNNUASMWGTM-UHFFFAOYSA-N
SMILES S1C=CN=C1C=O
LogP 0.602 (est)
CAS DataBase Reference 10200-59-6(CAS DataBase Reference)
UNSPSC Code 12352100
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H227-H315-H319-H335
Precautionary statements  P210-P280-P403+P235-P501-P210e-P261-P280a-P305+P351+P338-P405-P501a
Hazard Codes  Xn,Xi
Risk Statements  36/37/38-22
Safety Statements  36/37/39-26-23-36
WGK Germany  3
Hazard Note  Harmful
HS Code  29349990
Storage Class 10 - Combustible liquids
NFPA 704
2
2 0

1,3-Thiazole-2-carbaldehyde price More Price(32)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 422460 2-Thiazolecarboxaldehyde 97% 10200-59-6 1g $81.79 2025-07-31 Buy
TCI Chemical F0303 2-Formylthiazole >97.0%(GC) 10200-59-6 1g $39 2025-07-31 Buy
TCI Chemical F0303 2-Formylthiazole >97.0%(GC) 10200-59-6 5g $127 2025-07-31 Buy
Frontier Specialty Chemicals JK613181 2-Thiazolecarboxaldehyde 97% 10200-59-6 1g $98 2021-12-16 Buy
Matrix Scientific 069072 Thiazole-2-carboxaldehyde 98% 10200-59-6 25g $119 2021-12-16 Buy
Product number Packaging Price Buy
422460 1g $81.79 Buy
F0303 1g $39 Buy
F0303 5g $127 Buy
JK613181 1g $98 Buy
069072 25g $119 Buy

1,3-Thiazole-2-carbaldehyde Chemical Properties,Uses,Production

Chemical Properties

Colorless to light yellow liqui

Uses

2-Thiazolecarboxaldehyde is a useful building block for taxane analogs.

Synthesis Reference(s)

Synthesis, p. 998, 1987 DOI: 10.1055/s-1987-28146

General Description

2-Thiazolecarboxaldehyde is a thiazole aldehyde derivative. It undergoes Baylis–Hillman reaction with methyl acrylate catalyzed by DABCO (1,4-diazabicyclo[2.2.2]octane). The reaction mechanism has been studied by electrospray ionization mass spectrometry (ESI-MS).

Synthesis

2-Bromothiazole

3034-53-5

N,N-Dimethylformamide

68-12-2

1,3-Thiazole-2-carbaldehyde

10200-59-6

General procedure for the synthesis of 2-formylthiazole from 2-bromothiazole and N,N-dimethylformamide: An ether (43 mL) solution of 2-bromothiazole (10.00 g, 60.96 mmol) was added dropwise to a cooled solvate over a period of 1 hr at -78°C. Subsequently, 1.6 M butyl lithium (46 mL, 73.5 mmol) in hexane was added. The resulting mixture was stirred at -70 °C for 20 min, and then N,N-dimethylformamide (7.50 mL, 97.5 mmol) was added over 1 h while keeping the temperature below -65 °C. The reaction was carried out at -65 °C. The reaction mixture was warmed to -40°C over 1 hr and stirring was continued at this temperature for 1 hr. The reaction mixture was slowly warmed to 0 °C and quenched with 4 M aqueous hydrochloric acid. The organic and aqueous layers were separated. The organic layer was washed with 4M aqueous hydrochloric acid solution and discarded. The combined aqueous layers were neutralized with potassium carbonate and extracted with ether (3 times). The combined organic extracts were dried over magnesium sulfate, filtered, and the solvent was removed in vacuum to give 2-formylthiazole (6.88 g, 99% yield) as a brown oil, which did not require further purification.

References

[1] Patent: WO2006/92268, 2006, A1. Location in patent: Page/Page column 22
[2] Journal of Organic Chemistry, 1995, vol. 60, # 15, p. 4749 - 4754
[3] Patent: US5512575, 1996, A
[4] Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences, 2007, vol. 62, # 12, p. 1525 - 1529
[5] Patent: WO2018/108125, 2018, A1. Location in patent: Paragraph 00539

3034-53-5
10200-59-6
Synthesis of 1,3-Thiazole-2-carbaldehyde from 2-Bromothiazole
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View Lastest Price from 1,3-Thiazole-2-carbaldehyde manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
1,3-Thiazole-2-carbaldehyde pictures 2025-06-06 1,3-Thiazole-2-carbaldehyde
10200-59-6
US $768.00-15000.00 / kg 1kg 99% 10mt Sach biotech Co.,Ltd
1,3-Thiazole-2-carbaldehyde pictures 2025-05-26 1,3-Thiazole-2-carbaldehyde
10200-59-6
US $5.00-2.00 / KG 1KG 99% 10000kg Hebei Chuanghai Biotechnology Co,.LTD
1,3-Thiazole-2-carbaldehyde pictures 2024-07-23 1,3-Thiazole-2-carbaldehyde
10200-59-6
US $0.00-0.00 / kg 1kg 99% 10ton JINING XINHE CHEMICAL CO., LTD
2-THIAZOLECARBOXALDEHYDE 2-THIAZOLECARBOXYALDEHYDE THIAZOLE-2-CARBOXALDEHYDE 1,3-Thiazole-2-carboxaldehyde 2-ThiazoleCarboxaldehyde(=2-FormylThiazole) 2-FORMYLTHIAZOLE 1,3-THIAZOLE-2-CARBALDEHYDE 1,3-Thiazole-2-carboxaldehyde 95% 2-THIOZOLE CARBOXALDEHYDE 2-Thiazolecarboxaldehyde ,97% 2-Thiazolecarbaldehyde 1,3-Thiazole-2-Carbaldehyd 2-Thiazolecarboxaldehyde,98% 1,3-Thiazole-2-carboxaldehyde 95+% 2-Formyl-1,3-thiazole thiazol-2-carbaldehyde 2-Thiazolecarboxaldehyde 97% EOS-61959 2-Formylthiazole> 20:5n3) eicosapentaenoate (EPA 1,3-Thiazole-2-carbaldehyde ISO 9001:2015 REACH THIAZOLE-2-CARBALDEHYDE 2-Thiazolecarboxaldehyde (6CI, 7CI, 8CI, 9CI, ACI) 10200-59-6 C4H3NOS Heterocyclic Building Blocks Thiazoles Building Blocks Thiazole Thiazoles, Isothiazoles & Benzothiazoles Boronic Acid Heterocyclic Compounds Building Blocks Heterocyclic Building Blocks Aldehydes Thiazoles, Isothiazoles &Benzothiazoles API Thiazoles Building Blocks