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4-Hydroxymethylthiazole

CAS No.
7036-04-6
Chemical Name:
4-Hydroxymethylthiazole
Synonyms
4-Thiazolemethanol;THIAZOLE-4-METHANOL;4-Hydroxymethylthiaz;4-HYDROXYMETHYLTHIAZOLE;1,3-THIAZOL-4-YLMETHANOL;4-(Hydroxymethyl)-1,3-thiazole;4-(Hydroxymethyl)-1,3-thiazole95%;4-(Hydroxymethyl)-1,3-thiazole 95%;4-HydroxyMethylthiazole CAS7036-04-6
CBNumber:
CB9672002
Molecular Formula:
C4H5NOS
Molecular Weight:
115.15
MDL Number:
MFCD04115728
MOL File:
7036-04-6.mol
MSDS File:
SDS
Last updated:2025-07-24 18:13:53

4-Hydroxymethylthiazole Properties

Melting point 112-114 °C(Solv: ethyl ether (60-29-7); ethanol (64-17-5))
Boiling point 85-90/0.5mm
Density 1.339±0.06 g/cm3(Predicted)
storage temp. 2-8°C
form liquid
pka 13.21±0.10(Predicted)
color colourless
InChI InChI=1S/C4H5NOS/c6-1-4-2-7-3-5-4/h2-3,6H,1H2
InChIKey WQVOUANKVCYEIQ-UHFFFAOYSA-N
SMILES S1C=C(CO)N=C1
CAS DataBase Reference 7036-04-6(CAS DataBase Reference)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P305+P351+P338
Hazard Codes  Xi
Risk Statements  37/38-41
Safety Statements  26-39
Hazard Note  Irritant
HS Code  2934100090

4-Hydroxymethylthiazole price More Price(27)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Matrix Scientific 069454 4-(Hydroxymethyl)thiazole 97% 7036-04-6 1g $72 2021-12-16 Buy
Apolloscientific OR5598 4-(Hydroxymethyl)-1,3-thiazole 95% 7036-04-6 1g $145 2021-12-16 Buy
SynQuest Laboratories 8H01-1-04 4-(Hydroxymethyl)-1,3-thiazole 95% 7036-04-6 1g $160 2021-12-16 Buy
AK Scientific X0268 4-Hydroxymethylthiazole 7036-04-6 5g $289 2021-12-16 Buy
Apolloscientific OR5598 4-(Hydroxymethyl)-1,3-thiazole 95% 7036-04-6 5g $363 2021-12-16 Buy
Product number Packaging Price Buy
069454 1g $72 Buy
OR5598 1g $145 Buy
8H01-1-04 1g $160 Buy
X0268 5g $289 Buy
OR5598 5g $363 Buy

4-Hydroxymethylthiazole Chemical Properties,Uses,Production

Chemical Properties

Off-yellow oily liquid

Synthesis

ETHYL THIAZOLE-4-CARBOXYLATE

14527-43-6

4-Hydroxymethylthiazole

7036-04-6

The general procedure for the synthesis of 4-hydroxymethylthiazole from ethyl 4-thiazolecarboxylate was as follows: - Lithium aluminum hydride (1M tetrahydrofuran solution, 1.5 mL) was slowly added dropwise to a stirred tetrahydrofuran solution (4 mL) of ethyl 4-thiazolecarboxylate (224 mg) at 0 °C. - The reaction mixture was naturally warmed to room temperature with stirring for 1 hour. - Ethyl acetate (20 mL), water (1 mL), 2M sodium hydroxide solution (2 mL), and water (3 mL) were added sequentially to the reaction mixture. - The precipitate formed was removed by filtration through diatomaceous earth (iT). - The filtrate was concentrated to give 4-hydroxymethylthiazole (150 mg, 92% yield). - Nuclear magnetic resonance hydrogen spectroscopy (DMSO-d6) data: δ 4.12 (s, 2H), 7.47 (s, 1H), 9.03 (s, 1H).

References

[1] Patent: WO2005/61465, 2005, A1. Location in patent: Page/Page column 62
[2] European Journal of Medicinal Chemistry, 2018, vol. 154, p. 367 - 391

3364-80-5
7036-04-6
Synthesis of 4-Hydroxymethylthiazole from Thiazole-4-carboxaldehyde
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4-Hydroxymethylthiazole Spectrum

4-Hydroxymethylthiaz 4-HydroxyMethylthiazole CAS7036-04-6 4-(Hydroxymethyl)-1,3-thiazole95% THIAZOLE-4-METHANOL 1,3-THIAZOL-4-YLMETHANOL 4-HYDROXYMETHYLTHIAZOLE 4-(Hydroxymethyl)-1,3-thiazole 4-(Hydroxymethyl)-1,3-thiazole 95% 4-Thiazolemethanol 7036-04-6 4/6/7036 1875-98-3 7036-4-6 blocks Thiazoles