Basic Information | Post buying leads | Suppliers | Cas Database |
Name |
4-(Bromomethyl)pyridine hydrobromide |
EINECS | 629-462-7 |
CAS No. | 73870-24-3 | Density | N/A |
PSA | 12.89000 | LogP | 2.93460 |
Solubility | Soluble in water | Melting Point |
189-192 °C(lit.) |
Formula | C6H6BrN.HBr | Boiling Point | N/A |
Molecular Weight | 252.936 | Flash Point | N/A |
Transport Information | UN 3261 | Appearance | N/A |
Safety | 26-36/37/39-45 | Risk Codes | 34 |
Molecular Structure | Hazard Symbols | C | |
Synonyms |
Pyridine,4-(bromomethyl)-, hydrobromide (6CI,9CI);(4-Pyridyl)methyl bromidehydrobromide;4-(Bromomethyl)pyridine hydrobromide;4-Picolyl bromidehydrobromide; |
Article Data | 7 |
4-(hydroxymethyl)pyridine hydrobromide
4-bromomethyl pyridine hydrobromide
Conditions | Yield |
---|---|
With phosphorus tribromide In chloroform at 45℃; | 93% |
With phosphorus tribromide In chloroform for 3h; Heating; | 91% |
With phosphorus tribromide In chloroform for 4.5h; Reflux; | 78% |
pyridine-4-methanol
4-bromomethyl pyridine hydrobromide
Conditions | Yield |
---|---|
With phosphorus pentabromide In chloroform | 58.1% |
With hydrogen bromide In water at 150℃; | 50% |
With hydrogen bromide In water for 8h; Product distribution / selectivity; Reflux; | |
Multi-step reaction with 2 steps 1: hydrogen bromide / water / 4 h / Reflux 2: phosphorus tribromide / chloroform / 4.5 h / Reflux View Scheme | |
Multi-step reaction with 2 steps 1: hydrogen bromide / 4 h / 100 °C 2: phosphorus tribromide / chloroform / 45 °C View Scheme |
pyridine-4-carbaldehyde
4-bromomethyl pyridine hydrobromide
Conditions | Yield |
---|---|
Multi-step reaction with 3 steps 1: sodium tetrahydroborate / methanol / 2 h / 0 - 25 °C 2: hydrogen bromide / 4 h / 100 °C 3: phosphorus tribromide / chloroform / 45 °C View Scheme |
4-bromomethyl pyridine hydrobromide
4-(2-azidomethyl)pyridine
Conditions | Yield |
---|---|
Stage #1: 4-bromomethyl pyridine hydrobromide With potassium carbonate In N,N-dimethyl-formamide for 0.25h; Stage #2: With sodium azide In N,N-dimethyl-formamide at 20℃; for 3h; | 100% |
Stage #1: 4-bromomethyl pyridine hydrobromide With potassium carbonate at 20℃; for 0.25h; Inert atmosphere; Stage #2: With sodium azide at 20℃; for 72h; Inert atmosphere; | 49% |
Stage #1: 4-bromomethyl pyridine hydrobromide With potassium carbonate In N,N-dimethyl-formamide for 0.25h; Stage #2: With sodium azide In N,N-dimethyl-formamide at 20℃; for 4h; |
Conditions | Yield |
---|---|
With caesium carbonate In N,N-dimethyl-formamide at 20℃; for 1h; | 100% |
4-bromomethyl pyridine hydrobromide
Conditions | Yield |
---|---|
With caesium carbonate In N,N-dimethyl-formamide at 20℃; for 1h; | 99% |
N-{3-[(4-fluorobenzyl)oxy]phenyl}piperidine-4-carboxamide hydrochloride
4-bromomethyl pyridine hydrobromide
N-{3-[(4-fluorobenzyl)oxy]phenyl}-1-(pyridin-4-ylmethyl)piperidine-4-carboxamide
Conditions | Yield |
---|---|
With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 48h; | 97% |
4-bromomethyl pyridine hydrobromide
Conditions | Yield |
---|---|
With lithium hexamethyldisilazane In tetrahydrofuran at -78℃; for 2h; | 96.53% |
Stage #1: tert-butyl 2-(4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl)acetate With lithium hexamethyldisilazane In tetrahydrofuran at -78℃; for 0.333333h; Inert atmosphere; Stage #2: 4-bromomethyl pyridine hydrobromide In tetrahydrofuran at -78 - 20℃; for 2h; | |
Stage #1: tert-butyl 2-(4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl)acetate With lithium hexamethyldisilazane In tetrahydrofuran at -78℃; for 0.333333h; Inert atmosphere; Stage #2: 4-bromomethyl pyridine hydrobromide In tetrahydrofuran at -78 - 20℃; for 2h; | |
Stage #1: tert-butyl 2-(4-(5-chloro-2-cyanophenyl)-5-methoxy-2-oxopyridin-1(2H)-yl)acetate With lithium hexamethyldisilazane In tetrahydrofuran at -78℃; for 0.333333h; Inert atmosphere; Stage #2: 4-bromomethyl pyridine hydrobromide at -78 - 20℃; for 2h; |
(S)-(+)-(2,2-dimethyl-[1,3]dioxolan-4-yl)methanol
4-bromomethyl pyridine hydrobromide
Conditions | Yield |
---|---|
Stage #1: (S)-(+)-(2,2-dimethyl-[1,3]dioxolan-4-yl)methanol With sodium hydride In tetrahydrofuran; N,N-dimethyl-formamide; mineral oil at 0℃; for 0.333333h; Inert atmosphere; Schlenk technique; Stage #2: 4-bromomethyl pyridine hydrobromide In tetrahydrofuran; N,N-dimethyl-formamide; mineral oil at 0 - 20℃; for 0.5h; Inert atmosphere; Schlenk technique; | 95% |
4-bromomethyl pyridine hydrobromide
Conditions | Yield |
---|---|
Stage #1: 3,6-bis(5-(4,4,5,5-tetramethyl-1,3-dioxolan-2-yl)thiophen-2-yl)-9H-carbazole With sodium hydride In tetrahydrofuran; mineral oil at 0℃; Inert atmosphere; Schlenk technique; Stage #2: 4-bromomethyl pyridine hydrobromide With potassium carbonate In tetrahydrofuran; diethyl ether; water; mineral oil at 20℃; Inert atmosphere; Schlenk technique; | 91% |
The 4-(Bromomethyl)pyridine hydrobromide, with CAS registry number 73870-24-3, belongs to the following product categories: (1)Heterocyclic Building Blocks; (2)Halogenated Heterocycles; (3)Pyridines. It has the systematic name of 4-(bromomethyl)pyridine hydrobromide (1:1). And the chemical formula of this chemical is C6H6BrN.HBr.
When you are using this chemical, please be cautious about it as the following:
The 4-(Bromomethyl)pyridine hydrobromide may cause burns. When use it, wear suitable protective clothing, gloves and eye/face protection. If contact with eyes, rinse immediately with plenty of water and seek medical advice.
You can still convert the following datas into molecular structure:
(1)SMILES: c1cnccc1CBr.Br
(2)InChI: InChI=1/C6H6BrN.BrH/c7-5-6-1-3-8-4-2-6;/h1-4H,5H2;1H
(3)InChIKey: VAJUUDUWDNCECT-UHFFFAOYAF
(4)Std. InChI: InChI=1S/C6H6BrN.BrH/c7-5-6-1-3-8-4-2-6;/h1-4H,5H2;1H
(5)Std. InChIKey: VAJUUDUWDNCECT-UHFFFAOYSA-N