| Identification | More | [Name]
4-BROMOBUTYRYL CHLORIDE | [CAS]
927-58-2 | [Synonyms]
4-BROMOBUTYRYL CHLORIDE
G-BROMOBUTYROYL CHLORIDE
4-Bromobutanoyl chloride
4-bromo-butanoylchlorid
Butyryl chloride, 4-bromo-
gamma-Bromobutyroyl chloride
gamma-Bromobutyryl chloride
4-Bromobutyrylchloride,97%
4-Bromobutanoic acid chloride | [EINECS(EC#)]
213-154-0 | [Molecular Formula]
C4H6BrClO | [MDL Number]
MFCD00000753 | [Molecular Weight]
185.45 | [MOL File]
927-58-2.mol |
| Chemical Properties | Back Directory | [Appearance]
clear colorless to slightly yellow or | [Boiling point ]
101 °C37 mm Hg(lit.)
| [density ]
1.60 g/mL at 20 °C
| [refractive index ]
n20/D 1.492(lit.)
| [Fp ]
91 °C
| [storage temp. ]
2-8°C
| [form ]
Liquid | [color ]
Clear colorless to slightly yellow or light pink | [Water Solubility ]
Miscible with organic solvents. Immiscible with water. | [Sensitive ]
Moisture Sensitive | [BRN ]
1743026 | [InChI]
InChI=1S/C4H6BrClO/c5-3-1-2-4(6)7/h1-3H2 | [InChIKey]
LRTRXDSAJLSRTG-UHFFFAOYSA-N | [SMILES]
C(Cl)(=O)CCCBr | [CAS DataBase Reference]
927-58-2(CAS DataBase Reference) | [NIST Chemistry Reference]
Butanoyl chloride, 4-bromo-(927-58-2) | [EPA Substance Registry System]
927-58-2(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
C | [Risk Statements ]
R14:Reacts violently with water.
R34:Causes burns.
R37:Irritating to the respiratory system. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . | [RIDADR ]
UN 3265 8/PG 2
| [WGK Germany ]
3
| [F ]
3-8-10 | [TSCA ]
Yes | [HazardClass ]
8 | [PackingGroup ]
II | [HS Code ]
29159000 |
| Hazard Information | Back Directory | [Chemical Properties]
clear colorless to slightly yellow or | [Uses]
4-Bromobutyryl chloride is used as a precursor for the synthesis of carolic acid by reacting with ethoxymagnesiomalonic ester. It is widely utilized as an intermediate in organic synthesis and pharmaceuticals. | [reaction suitability]
reagent type: cross-linking reagent |
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