| Identification | Back Directory | [Name]
2-METHOXY-5-NITROBENZYL BROMIDE | [CAS]
3913-23-3 | [Synonyms]
MNBB
KOSHLAND II
KOSHLANDREAGENTII
Koshland II reagent
koshlandreagentno.2
KOSHLAND'S REAGENT II
2-BROMOMETHYL-4-NITROANISOLE
2-(bromomethyl)-4-nitro-anisol
2-METHOXY-5-NITROBENZYL BROMIDE
2-Methoxy-5-nitrobenzyl bromide 97%
alpha-bromo-2-methoxy-6-nitro-toluen
2-Bromomethyl-1-methoxy-4-nitrobenzene
2-(bromomethyl)-1-methoxy-4-nitro-benzen
1-Methoxy-2-(bromomethyl)-4-nitrobenzene
Benzene, 2-(bromomethyl)-1-methoxy-4-nitro-
2-Bromomethyl-4-nitroanisole, Koshlands Reagent II | [EINECS(EC#)]
223-471-6 | [Molecular Formula]
C8H8BrNO3 | [MDL Number]
MFCD00007329 | [MOL File]
3913-23-3.mol | [Molecular Weight]
246.06 |
| Chemical Properties | Back Directory | [Melting point ]
76-78 °C(lit.)
| [Boiling point ]
348.7±27.0 °C(Predicted) | [density ]
1.589±0.06 g/cm3 (20 ºC 760 Torr) | [storage temp. ]
Inert atmosphere,2-8°C |
| Hazard Information | Back Directory | [Uses]
2-Methoxy-5-nitrobenzyl bromide was used to modify tryptophan residues of mouse interferon to enhance their activity. It was also used as reagent for sulfhydryl modification. | [General Description]
2-Methoxy-5-nitrobenzyl bromide is a potential mechanism-based inactivator of enzymes that perform O-dealkylations. | [Biochem/physiol Actions]
2-Methoxy-5-nitrobenzyl bromide inactivates cytochrome P-450 in male rat liver microsomes. |
|
| Company Name: |
Energy Chemical
|
| Tel: |
021-021-58432009 400-005-6266 |
| Website: |
http://www.energy-chemical.com |
| Company Name: |
Sigma-Aldrich
|
| Tel: |
021-61415566 800-8193336 |
| Website: |
https://www.sigmaaldrich.cn |
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