1,3-Thiazol-2-ylmethanol

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CAS:14542-12-2
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CAS:14542-12-2
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1,3-Thiazol-2-ylmethanol manufacturers

1,3-Thiazol-2-ylmethanol Basic information
Product Name:1,3-Thiazol-2-ylmethanol
Synonyms:RARECHEM AL BD 0750;1,3-THIAZOL-2-YLMETHANOL;2-HYDROXYMETHYLTHIAZOLE;2-THIAZOLEMETHANOL;2-(Hydroxymethyl)-1,3-thiazole;2-(Hydroxymethyl)-1,3-thiazole 97%;THIAZOL-2-YL-METHANOL;2-(Hydroxylmethyl)thiazole
CAS:14542-12-2
MF:C4H5NOS
MW:115.15
EINECS:696-096-2
Product Categories:Building Blocks;Thiazole;Thiazoles, Isothiazoles & Benzothiazoles;Thiazole series;Hydroxymethyl's;Thiazoles, Isothiazoles &Benzothiazoles;API intermediates
Mol File:14542-12-2.mol
1,3-Thiazol-2-ylmethanol Structure
1,3-Thiazol-2-ylmethanol Chemical Properties
Melting point 62-64.5
Boiling point 76°C/0.2mmHg(lit.)
density 1.339±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka12.87±0.10(Predicted)
form powder to crystal
color White to Orange to Green
CAS DataBase Reference14542-12-2(CAS DataBase Reference)
Safety Information
Hazard Codes Xn
Risk Statements 20/21/22-36/37/38
Safety Statements 22-26-36/37/39
Hazard Note Harmful
HS Code 2934100090
MSDS Information
1,3-Thiazol-2-ylmethanol Usage And Synthesis
Chemical Propertieswhite to light yellow crystal powde
Uses1,3-Thiazol-2-ylmethanol is a reagent used in the synthesis of quinazoline analogs which is an anti-proliferative activities and EGFR inhibitory potency.
Synthesis
1,3-Thiazole-2-carbaldehyde

10200-59-6

1,3-Thiazol-2-ylmethanol

14542-12-2

General procedure for the synthesis of 2-hydroxymethylthiazole from 2-formylthiazole: Thiazole-2-carbaldehyde (301 mg, 2.66 mmol) was dissolved in methanol (15 mL) at 0 °C. Subsequently, sodium borohydride (151 mg, 3.99 mmol) was slowly added to the reaction system and the reaction was continuously stirred for 2 h at this temperature. Upon completion of the reaction, the reaction mixture was poured into water (10 mL) to terminate the reaction. The solvent was removed by rotary evaporator and the resulting residue was extracted with ethyl acetate (15 mL x 3). The organic phases were combined, washed with saturated saline (15 mL) and dried over anhydrous sodium sulfate. After filtration, the organic solvent was removed by concentration under reduced pressure, and the crude product obtained was purified by column chromatography (eluent: petroleum ether/ethyl acetate, 5:1, v/v/v/v), and finally 285 mg of a light yellow oily product was obtained with a yield of 93%.

References[1] Chinese Journal of Chemistry, 2014, vol. 32, # 6, p. 538 - 544
[2] Patent: CN106749268, 2017, A. Location in patent: Paragraph 0798; 0799
[3] European Journal of Organic Chemistry, 2017, vol. 2017, # 33, p. 4972 - 4983
[4] Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences, 2007, vol. 62, # 12, p. 1525 - 1529
[5] Tetrahedron, 1988, vol. 44, # 7, p. 2021 - 2032
1,3-Thiazol-2-ylmethanol Preparation Products And Raw materials
Raw materials1,3-Thiazole-2-carbaldehyde-->Sodium borohydride-->Methanol
Tag:1,3-Thiazol-2-ylmethanol(14542-12-2) Related Product Information
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