| Identification | Back Directory | [Name]
9-FLUORENYLMETHYL N-(2-AMINOETHYL)CARBAMATE HYDROBROMIDE | [CAS]
352351-55-4 | [Synonyms]
N-FMOC-ETHYLENEDIAMINE HYDROBROMIDE N-FMOC-1,2-DIAMINOETHANE HYDROBROMIDE 9-FLUORENYLMETHYL N-(2-AMINOETHYL)CARBAMATE HYDROBROMIDE | [Molecular Formula]
C17H19BrN2O2 | [MDL Number]
MFCD01863041 | [MOL File]
352351-55-4.mol | [Molecular Weight]
363.26 |
| Chemical Properties | Back Directory | [Melting point ]
~165 °C (dec.) | [storage temp. ]
2-8°C | [form ]
solid | [InChI]
1S/C17H18N2O2.BrH/c18-9-10-19-17(20)21-11-16-14-7-3-1-5-12(14)13-6-2-4-8-15(13)16;/h1-8,16H,9-11,18H2,(H,19,20);1H | [InChIKey]
KZRZVRGZNSCCBV-UHFFFAOYSA-N | [SMILES]
NCCNC(OCC1C2=C(C=CC=C2)C3=C1C=CC=C3)=O.[H]Br |
| Hazard Information | Back Directory | [Uses]
N-Fmoc-ethylenediamine hydrobromide is an important chemical reagent with the activity of promoting organic synthesis reactions. N-Fmoc-ethylenediamine hydrobromide is often used in the synthesis of peptides and other amino compounds in the field of biochemistry because it can effectively protect the amino group and provide good reactivity. The application of N-Fmoc-ethylenediamine hydrobromide helps to improve the efficiency and selectivity of synthesis and becomes a key component in organic synthesis. | [reaction suitability]
reagent type: cross-linking reagent |
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