ChemicalBook--->CAS DataBase List--->20949-84-2

20949-84-2

20949-84-2 Structure

20949-84-2 Structure
IdentificationBack Directory
[Name]

4-FORMYL-2-METHYLTHIAZOLE
[CAS]

20949-84-2
[Synonyms]

IFLAB-BB F2124-0689
4-FORMYL-2-METHYLTHIAZOLE
2-Methyl-4-forMylthiazole
4-Formyl-2-methyl-1,3-thiazole
2-Methyl-4-thiazolecarbaldehyde
2-Methyl-4-thiazolecarboxaldehyde
2-Methylthiazole-4-carboxaldehyde
4-THIAZOLECARBOXALDEHYDE, 2-METHYL-
2-METHYL-1,3-THIAZOLE-4-CARBALDEHYDE
2-Methyl-1,3-thiazole-4-carboxaldehyde
2-Methyl-1,3-thiazole-4-carboxaldehyde97%
2-Methyl-1,3-thiazole-4-carboxaldehyde 97%
2-Methylthiazole-4-carboxaldehyde
[EINECS(EC#)]

687-053-9
[Molecular Formula]

C5H5NOS
[MDL Number]

MFCD06655197
[MOL File]

20949-84-2.mol
[Molecular Weight]

127.16
Chemical PropertiesBack Directory
[Melting point ]

56-58
[Boiling point ]

219.0±13.0 °C(Predicted)
[density ]

1.270±0.06 g/cm3(Predicted)
[Fp ]

110℃
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[form ]

solid
[pka]

1.22±0.10(Predicted)
[Appearance]

Off-white to yellow Solid
[InChI]

InChI=1S/C5H5NOS/c1-4-6-5(2-7)3-8-4/h2-3H,1H3
[InChIKey]

AEHWVNPVEUVPMT-UHFFFAOYSA-N
[SMILES]

S1C=C(C=O)N=C1C
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22
[WGK Germany ]

3
[Hazard Note ]

Harmful
[HS Code ]

2934100090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Hazard InformationBack Directory
[Chemical Properties]

Yellow Powder
[Synthesis]

	Ethyl 2-methylthiazole-4-carboxylate

6436-59-5

4-Formyl-2-methylthiazole

20949-84-2

The general procedure for the synthesis of 2-methyl-4-thiazolecarboxaldehyde using ethyl 2-methylthiazole-4-carboxylate as starting material was as follows: to a solution of ethyl 2-methylthiazole-4-carboxylate (1.00 g, 5.8 mmol) in toluene (18 mL) was slowly added dropwise to a solution of diisobutylaluminum hydroxide in dichloromethane (11.1 mL, 1 M) at -78 °C. After the dropwise addition was completed, the reaction system was kept at -78 °C and stirring was continued for 4 hours. Subsequently, the reaction was quenched by the addition of acetic acid (0.46 mL) and concentrated by slowly warming the reaction mixture to 25 °C. The concentrated residue was treated with dichloromethane and Rochelle's salt with vigorous stirring until a clarified two-phase solution was formed (about 10 min). The organic and aqueous layers were separated, and the organic layer was washed sequentially with 10% NaHCO3 solution and saturated saline, then dried with anhydrous Na2SO4, filtered and concentrated. Finally, the residue was purified by silica gel column chromatography, using 14% ethyl acetate in hexane solution as eluent, to obtain the target product 2-methyl-4-thiazolecarboxaldehyde (0.28 g, 38% yield).

[References]

[1] Organic Letters, 2008, vol. 10, # 8, p. 1565 - 1568
[2] Angewandte Chemie - International Edition in English, 1997, vol. 36, # 1-2, p. 166 - 168
[3] Journal of the American Chemical Society, 1997, vol. 119, # 34, p. 7974 - 7991
[4] Organic Letters, 2012, vol. 14, # 24, p. 6354 - 6357
[5] Angewandte Chemie - International Edition, 2000, vol. 39, # 1, p. 209 - 213
Spectrum DetailBack Directory
[Spectrum Detail]

4-Formyl-2-methylthiazole(20949-84-2)1HNMR
4-Formyl-2-methylthiazole(20949-84-2)1HNMR
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