| Identification | More | [Name]
2,6-Dibromoaniline | [CAS]
608-30-0 | [Synonyms]
2,6-DIBROMOANILINE
2,6-DIBROMO-PHENYLAMINE
2,6-Dibromobenzenamine
2,6-dibromo-Benzenamine
Aniline, 2,6-dibromo-
Benzenamine,2,6-dibromo-
Dibromoaniline
2,6-Dibromoaniline,97+%
2,6-Dibromanilin | [EINECS(EC#)]
210-158-4 | [Molecular Formula]
C6H5Br2N | [MDL Number]
MFCD00007638 | [Molecular Weight]
250.92 | [MOL File]
608-30-0.mol |
| Chemical Properties | Back Directory | [Appearance]
white to pale yellow or grey crystalline powder | [Melting point ]
80-82 °C (lit.) | [Boiling point ]
262-264 °C (lit.) | [density ]
1.9318 (rough estimate) | [refractive index ]
1.5800 (estimate) | [Fp ]
262-264°C | [storage temp. ]
Keep in dark place,Sealed in dry,Room Temperature | [solubility ]
Chloroform, Methanol | [form ]
Crystalline Powder | [pka]
0.48±0.10(Predicted) | [color ]
White to pale yellow or gray | [Water Solubility ]
Insoluble in water. | [Detection Methods]
NMR | [BRN ]
2207094 | [InChI]
1S/C6H5Br2N/c7-4-2-1-3-5(8)6(4)9/h1-3H,9H2 | [InChIKey]
XIRRDAWDNHRRLB-UHFFFAOYSA-N | [SMILES]
Nc1c(Br)cccc1Br | [CAS DataBase Reference]
608-30-0(CAS DataBase Reference) | [NIST Chemistry Reference]
Benzenamine, 2,6-dibromo-(608-30-0) |
| Safety Data | Back Directory | [Symbol(GHS) ]
GHS07 | [Signal word ]
Warning | [Hazard statements ]
H315-H317-H319-H335 | [Precautionary statements ]
P280-P302+P352-P305+P351+P338 | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [RIDADR ]
2811 | [WGK Germany ]
3
| [F ]
10 | [HazardClass ]
6.1 | [PackingGroup ]
III | [HS Code ]
29214200 | [Storage Class]
11 - Combustible Solids | [Hazard Classifications]
Eye Irrit. 2
Skin Irrit. 2
Skin Sens. 1
STOT SE 3 |
| Hazard Information | Back Directory | [Chemical Properties]
white to pale yellow or grey crystalline powder | [Uses]
2,5-Dibromoaniline was used in the synthesis of 2,4,5-tribromoaniline1. It was also used as starting reagent in the regioselective synthesis of 2-(3,4-dimethoxyphenyl)-5-bromobenzothiazole. |
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