| Identification | More | [Name]
2-Acetyl-5-bromothiophene | [CAS]
5370-25-2 | [Synonyms]
1-(5-BROMO-2-THIENYL)ETHAN-1-ONE
2-ACETYL-5-BROMOTHIOPHENE
5-BROMO-2-THIENYL METHYL KETONE
AKOS 93373
BUTTPARK 52\12-17
LABOTEST-BB LT01138486
1-(5-Bromo-2-thienyl)ethanone
1-(5-Bromo-thiophen-2-yl)-ethanone
2-Acetyl-5-bromthiophen
5-Bromo 2-acetylthiophene
Ethanone, 1-(5-bromo-2-thienyl)-
Ethanone,1-(5-bromo-2-thienyl)-
Ketone, 5-bromo-2-thienyl methyl
2-Acetyl-5-Bromo Thiophenone
2-ACETYL-5-BROMOTHIOPHENE ,98%
1-(5-Bromothiophene-2-yl)ethanone
2-Bromo-5-acetylthiophene
5-Acetyl-2-bromothiophene
Methyl(5-bromo-2-thienyl) ketone | [EINECS(EC#)]
226-363-7 | [Molecular Formula]
C6H5BrOS | [MDL Number]
MFCD00014528 | [Molecular Weight]
205.07 | [MOL File]
5370-25-2.mol |
| Chemical Properties | Back Directory | [Appearance]
white to light yellow crystal powder | [Melting point ]
94-96 °C (lit.) | [Boiling point ]
103 °C/4 mmHg (lit.) | [density ]
1.649 (estimate) | [Fp ]
103°C/4mm | [storage temp. ]
under inert gas (nitrogen or Argon) at 2–8 °C | [solubility ]
soluble in Methanol | [form ]
Crystalline Flakes or Powder | [color ]
Yellow | [Sensitive ]
Light Sensitive | [BRN ]
113949 | [InChIKey]
IGBZCOWXSCWSHO-UHFFFAOYSA-N | [CAS DataBase Reference]
5370-25-2(CAS DataBase Reference) | [NIST Chemistry Reference]
2-Acetyl-5-bromothiophene(5370-25-2) |
| Safety Data | Back Directory | [Hazard Codes ]
Xn | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin .
R20/21/22:Harmful by inhalation, in contact with skin and 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 .
S22:Do not breathe dust . | [RIDADR ]
UN2811 | [WGK Germany ]
3
| [HazardClass ]
LIGHT SENSITIVE | [HS Code ]
29339900 |
| Hazard Information | Back Directory | [Chemical Properties]
white to light yellow crystal powder | [Uses]
2-Acetyl-5-bromothiophene was used as a starting reagent in the synthesis of bithiophene bis-imidazo[1,2-a]pyridine derivatives. It was also used in the preparation of phosphorus-containing fused bicyclic 5,6-membered compounds. | [Synthesis Reference(s)]
Journal of Heterocyclic Chemistry, 18, p. 1345, 1981 DOI: 10.1002/jhet.5570180714
Synthetic Communications, 11, p. 29, 1981 DOI: 10.1080/00397918108064279 |
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