ChemicalBook > CAS DataBase List > 4-AZIDOPHENACYL BROMIDE
4-AZIDOPHENACYL BROMIDE
4-AZIDOPHENACYL BROMIDE
- CAS No.57018-46-9
- Chemical Name:4-AZIDOPHENACYL BROMIDE
- CBNumber:CB3120420
- Molecular Formula:C8H6BrN3O
- Formula Weight:240.06
- MOL File:57018-46-9.mol
4-AZIDOPHENACYL BROMIDE Property
- Melting point 64-65 °C
- storage temp. 2-8°C
- solubility methanol: 50 mg/mL
- form powder
- color yellow
- BRN 1961705
- Stability Light, Temperature And Moisture Sensitive, Temperature and Moisture sensitive
- FDA UNII POZ2E56V0Y
- UNSPSC Code 12352100
- NACRES NA.22
Safety
- Hazard Codes :F,C
- Risk Statements :11-34-42/43
- Safety Statements :16-26-27-36/37/39-45
- RIDADR :UN 1325 4.1/PG 2
- WGK Germany :3
- F :4.5-8-10-19
- HazardClass :4.1
- PackingGroup :III
- HS Code :29299090
-
Symbol(GHS)
- Signal wordDanger
- Hazard statements H228-H314-H317-H334
- Precautionary statements P210-P261-P280-P305+P351+P338-P310
4-AZIDOPHENACYL BROMIDE Chemical Properties,Usage,Production
- Chemical Properties 4-AZIDOPHENACYL BROMIDE is off-White Crystalline Solid
- Uses 4-AZIDOPHENACYL BROMIDE is a versatile photolabile bifunctional reagent. Useful for investigating the active sites of sulfhydryl enzymes-particularly those which posess a particularly reactive cysteine residue at the active site. Used to study the nature of the ribosomal binding site of E. coli tRNAVal.
- Uses Photoactive, heterobifunctional cross-linking reagent. Typically, the initial reaction couples to sulfhydryl in the pH range 7.0-8.0. Second bonding occurs during UV irradiation (250 nm) via reactive nitrene. The latter bonding is rapid and non-specific.
-
reaction suitability
reaction type: click chemistry
reagent type: cross-linking reagent
4-AZIDOPHENACYL BROMIDE Preparation Products And Raw materials
Raw materials
Preparation Products
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57018-46-9, 4-AZIDOPHENACYL BROMIDERelated Search:
- Sulfur & Selenium Compounds
- MTS & Sulfhydryl Active Reagents
- Aromatics
- Photoaffinity Labels
- Affinity Chromatography
- 4 4'-偶氮双(4-氰基戊酸
- Azides
- Building Blocks
- BioChemical
- Protein Modification
- Proteomics and Protein Expression
- Proteomics
- Nitrogen Compounds
- Organic Building Blocks
- Crosslinking
- Heterobifunctional Cross-Linking Reagents
- C8H6BrN3O
- C8H6N3OBr
- 对叠氮苯甲酰溴
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- 4-叠氮苯甲酰甲基溴
- 4′-叠氮-2-溴苯乙酮
- 57018-46-9
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