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2-METHOXY-5-NITROBENZYL BROMIDE
- Chemical Name: 2-METHOXY-5-NITROBENZYL BROMIDE
- CAS: 3913-23-3
- Purity: 99%
Reliable Quality 2-METHOXY-5-NITROBENZYL BROMIDE 3913-23-3 Hot Sale with Chinese Manufacturer We supply high quality 2-METHOXY-5-NITROBENZYL BROMIDE (CAS 3913-23-3), in stock, factory directly supply to clients, lower prices, more competitiveness.
What is the 2-METHOXY-5-NITROBENZYL BROMIDE ?
2-METHOXY-5-NITROBENZYL BROMIDE is UN 3261, while it's Molecular Formula is C8H8BrNO3. 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.
What is the CAS number for 2-METHOXY-5-NITROBENZYL BROMIDE ?
The CAS number of 2-METHOXY-5-NITROBENZYL BROMIDE is 3913-23-3.
More information of 2-METHOXY-5-NITROBENZYL BROMIDE 3913-23-3 are:
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Synonyms |
Anisole,2-(bromomethyl)-4-nitro- (7CI,8CI);2-(Bromomethyl)-1-methoxy-4-nitrobenzene;2-(Bromomethyl)-4-nitroanisole;2-Methoxy-5-nitrobenzyl bromide;Koshlandreagent 2;Koshland reagent No. 2;Koshland reagent number 2; |
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CAS?Number |
3913-23-3 |
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Molecular Formula |
C8H8BrNO3 |
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Molecular Weight |
246.06 |
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Density |
1.589g/cm3 |
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Melting Point |
76-78 °C(lit.) |
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Boiling Point |
348.7 °C at 760 mmHg |
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Flash Point |
164.7 °C |
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HS CODE |
2909309090 |
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PSA |
55.05000 |
|
LogP |
3.02150 |
What is 2-METHOXY-5-NITROBENZYL BROMIDE (3913-23-3) used for?
2-Methoxy-5-nitrobenzyl bromide is an organic compound that serves as a potential mechanism-based inactivator of enzymes involved in O-dealkylations. It is characterized by its ability to modify tryptophan residues and is utilized in various applications across different industries.
InChI:InChI=1/C8H8BrNO3/c1-13-8-3-2-7(10(11)12)4-6(8)5-9/h2-4H,5H2,1H3
Articles related to 2-METHOXY-5-NITROBENZYL BROMIDE:
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Article |
Source |
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THERAPEUTIC COMPOUNDS |
- Paragraph 0395; 0403; 0407, (2017/01/23) |
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Discovery of a clinical stage multi-kinase inhibitor sodium (E)-2-{2-methoxy-5-[(2′,4′,6′-trimethoxystyrylsulfonyl)methyl] phenylamino}acetate (ON 01910.Na): Synthesis, structure-activity relationship, and biological activity |
Reddy, M. V. Ramana,Venkatapuram, Padmavathi,Mallireddigari, Muralidhar R.,Pallela, Venkat R.,Cosenza, Stephen C.,Robell, Kimberly A.,Akula, Balaiah,Hoffman, Benjamin S.,Reddy, E. Premkumar experimental part, p. 6254 - 6276 (2011/11/01) |
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