| Identification | More | [Name]
1,3-Thiazole-2-carbaldehyde | [CAS]
10200-59-6 | [Synonyms]
1,3-THIAZOLE-2-CARBALDEHYDE
2-FORMYLTHIAZOLE
2-THIAZOLECARBOXALDEHYDE
2-THIAZOLECARBOXYALDEHYDE
THIAZOLE-2-CARBALDEHYDE
THIAZOLE-2-CARBOXALDEHYDE
1,3-Thiazole-2-carboxaldehyde
2-ThiazoleCarboxaldehyde(=2-FormylThiazole)
1,3-Thiazole-2-carboxaldehyde 95%
2-THIOZOLE CARBOXALDEHYDE
2-Thiazolecarboxaldehyde ,97%
2-Thiazolecarbaldehyde | [EINECS(EC#)]
688-154-0 | [Molecular Formula]
C4H3NOS | [MDL Number]
MFCD00142924 | [Molecular Weight]
113.14 | [MOL File]
10200-59-6.mol |
| Chemical Properties | Back Directory | [Appearance]
Colorless to light yellow liqui | [Boiling point ]
61-63 °C/15 mmHg (lit.) | [density ]
1.288 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.574(lit.)
| [Fp ]
154 °F
| [storage temp. ]
Refrigerator (+4°C) | [form ]
Liquid | [pka]
0.44±0.10(Predicted) | [color ]
Colorless to pale yellow | [Water Solubility ]
soluble | [Detection Methods]
GC | [InChIKey]
ZGTFNNUASMWGTM-UHFFFAOYSA-N | [LogP]
0.602 (est) | [CAS DataBase Reference]
10200-59-6(CAS DataBase Reference) | [Storage Precautions]
Store under nitrogen |
| Safety Data | Back Directory | [Hazard Codes ]
Xn,Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin .
R22:Harmful if swallowed. | [Safety Statements ]
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [Hazard Note ]
Harmful | [HS Code ]
29349990 |
| Hazard Information | Back Directory | [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). |
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