2-METHOXY-5-NITROBENZYL BROMIDE

2-METHOXY-5-NITROBENZYL BROMIDE Structure
CAS No.
3913-23-3
Chemical Name:
2-METHOXY-5-NITROBENZYL BROMIDE
Synonyms
MNBB;KOSHLAND II;KOSHLANDREAGENTII;koshlandreagentno.2;Koshland II reagent;KOSHLAND'S REAGENT II;2-BROMOMETHYL-4-NITROANISOLE;2-(bromomethyl)-4-nitro-anisol;2-METHOXY-5-NITROBENZYL BROMIDE;2-Methoxy-5-nitrobenzyl bromide 97%
CBNumber:
CB3704774
Molecular Formula:
C8H8BrNO3
Molecular Weight:
246.06
MOL File:
3913-23-3.mol
MSDS File:
SDS

2-METHOXY-5-NITROBENZYL BROMIDE Properties

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. under inert gas (nitrogen or Argon) at 2-8°C

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS05
Signal word  Danger
Hazard statements  H314
Precautionary statements  P280-P305+P351+P338-P310
Hazard Codes  C
Risk Statements  34
Safety Statements  26-27-36/37/39-45
RIDADR  UN 3261 8/PG 2
WGK Germany  3
RTECS  XS7966500
19-21
HazardClass  8
PackingGroup  III

2-METHOXY-5-NITROBENZYL BROMIDE Chemical Properties,Uses,Production

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.

2-METHOXY-5-NITROBENZYL BROMIDE Preparation Products And Raw materials

Raw materials

Preparation Products

2-METHOXY-5-NITROBENZYL BROMIDE Suppliers

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2-(bromomethyl)-1-methoxy-4-nitro-benzen 2-(bromomethyl)-4-nitro-anisol alpha-bromo-2-methoxy-6-nitro-toluen koshlandreagentno.2 2-BROMOMETHYL-4-NITROANISOLE 2-METHOXY-5-NITROBENZYL BROMIDE 2-Bromomethyl-4-nitroanisole, Koshlands Reagent II KOSHLAND II KOSHLAND'S REAGENT II Benzene, 2-(bromomethyl)-1-methoxy-4-nitro- KOSHLANDREAGENTII 1-Methoxy-2-(bromomethyl)-4-nitrobenzene 2-Bromomethyl-1-methoxy-4-nitrobenzene MNBB Koshland II reagent 2-Methoxy-5-nitrobenzyl bromide 97% 3913-23-3 CH3OC6H3NO2CH2Br C8H8NO3Br Building Blocks Nitrogen Compounds Organic Building Blocks Nitro Compounds Building Blocks Chemical Synthesis Nitro Compounds Nitrogen Compounds Organic Building Blocks