2-Bromopyridine-3-carbaldehyde supplier

Name
2-BROMO-3-FORMYLPYRIDINE
EINECS
CAS No. 128071-75-0
Article Data32
CAS DataBase
Density 1.683 g/cm³
Solubility
Melting Point 73 °C
Formula C₆H₄BrNO
Boiling Point 267.7 °C at 760 mmHg
Molecular Weight 186.008
Flash Point 115.7 °C
Transport Information
Appearance
Safety 26-36/37
Risk Codes 22-36-43
Molecular Structure
Hazard Symbols Xn,Xi
Synonyms 2-Bromo-3-pyridinecarboxaldehyde;2-Bromo-3-formylpyridine;2-Bromonicotinaldehyde;
PSA 29.96000
LogP 1.65660

Synthetic route

: 109-04-6
2-bromo-pyridine

: 68-12-2, 33513-42-7
N,N-dimethyl-formamide

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

Conditions

Conditions	Yield
Stage #1: 2-bromo-pyridine With lithium diisopropyl amide In tetrahydrofuran at -78℃; for 3h; Stage #2: N,N-dimethyl-formamide In tetrahydrofuran at -78℃; for 1h; Further stages.;	85%
Stage #1: 2-bromo-pyridine With lithium diisopropyl amide In tetrahydrofuran at -50℃; for 1h; Stage #2: N,N-dimethyl-formamide In tetrahydrofuran for 1h; Temperature; Reagent/catalyst;	78%
Stage #1: 2-bromo-pyridine With lithium diisopropyl amide In tetrahydrofuran; hexane at -78℃; for 4h; Inert atmosphere; Stage #2: N,N-dimethyl-formamide In tetrahydrofuran; hexane at -78℃; for 0.5h; Inert atmosphere;	75%

: 131747-54-1
(2-bromopyrid-3-yl)methanol

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

Conditions

Conditions	Yield
With phosphoric acid; dimethyl sulfoxide; dicyclohexyl-carbodiimide for 1.5h; Ambient temperature;	83%
With phosphoric acid; dimethyl sulfoxide; dicyclohexyl-carbodiimide at 20℃; for 1.5h;	80%

: 865449-15-6
2-bromo-3-(dibromomethyl)-pyridine

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

Conditions

Conditions	Yield
With calcium carbonate In water for 8h; Heating;	83%
With calcium carbonate In water for 14h; Reflux;	78%
With water; calcium carbonate at 100℃; for 7h;	60%

: 109-04-6
2-bromo-pyridine

: 50-00-0
formaldehyd

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

Conditions

Conditions	Yield
With lithium	42%

: 109-04-6
2-bromo-pyridine

: 109-94-4
formic acid ethyl ester

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

Conditions

Conditions	Yield
Stage #1: 2-bromo-pyridine With lithium diisopropyl amide In tetrahydrofuran at -78℃; for 2h; Stage #2: formic acid ethyl ester In tetrahydrofuran at -78℃; for 1h; Stage #3: With water; ammonium chloride In tetrahydrofuran at -30℃;	11%

: 626-05-1
2,6-Dibromopyridine

: 68-12-2, 33513-42-7
N,N-dimethyl-formamide

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

Conditions

Conditions	Yield
Yield given. Multistep reaction;

: 58530-53-3
2,4-dibromopyridine

: 68-12-2, 33513-42-7
N,N-dimethyl-formamide

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

Conditions

Conditions	Yield
Yield given. Multistep reaction;

: 624-28-2
2,5-dibromopyridine

: 68-12-2, 33513-42-7
N,N-dimethyl-formamide

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

Conditions

Conditions	Yield
Yield given. Multistep reaction;

: 1036408-89-5
C9H8BrNO4

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 1.03 g / LiAlH4 / tetrahydrofuran / 0.5 h / -78 °C 2: 80 percent / N,N'-dicyclohexylcarbodiimide; H3PO4; DMSO / 1.5 h / 20 °C View Scheme

: 3430-17-9
2-bromo-3-picoline

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

Conditions

Conditions	Yield
Multi-step reaction with 4 steps 1: 98 percent / KMnO4; H2O / 20 h / Heating 2: Et3N / benzene / 1 h / 20 °C 3: 1.03 g / LiAlH4 / tetrahydrofuran / 0.5 h / -78 °C 4: 80 percent / N,N'-dicyclohexylcarbodiimide; H3PO4; DMSO / 1.5 h / 20 °C View Scheme
Multi-step reaction with 2 steps 1: 83 percent / N-bromosuccinimide; benzoylperoxyde / CCl4 / 4 h / Heating 2: 83 percent / CaCO3 / H2O / 8 h / Heating View Scheme
Multi-step reaction with 3 steps 1: 70 percent / KMnO4 / H2O / Heating 2: 1) NEt3, ethyl chloroformate, 2) LiAlH4 / 1) benzene, rt, 1 h, 2) THF, -78 deg C, 30 min 3: 83 percent / DMSO, N,N'-dicyclohexylcarbodiimide, H3PO4 / 1.5 h / Ambient temperature View Scheme
Multi-step reaction with 2 steps 1: N-Bromosuccinimide; dibenzoyl peroxide / dichloromethane / 4 h / 80 °C / Inert atmosphere 2: calcium carbonate; water / 7 h / 100 °C View Scheme
Multi-step reaction with 2 steps 1: N-Bromosuccinimide; dibenzoyl peroxide / tetrachloromethane / 4 h / Reflux 2: calcium carbonate / water / 14 h / Reflux View Scheme

: 35905-85-2
2-bromonicotinic acid

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: Et3N / benzene / 1 h / 20 °C 2: 1.03 g / LiAlH4 / tetrahydrofuran / 0.5 h / -78 °C 3: 80 percent / N,N'-dicyclohexylcarbodiimide; H3PO4; DMSO / 1.5 h / 20 °C View Scheme
Multi-step reaction with 2 steps 1: 1) NEt3, ethyl chloroformate, 2) LiAlH4 / 1) benzene, rt, 1 h, 2) THF, -78 deg C, 30 min 2: 83 percent / DMSO, N,N'-dicyclohexylcarbodiimide, H3PO4 / 1.5 h / Ambient temperature View Scheme

: 1603-40-3
3-methylpyridin-2-ylamine

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1.1: HBr; Br2 / H2O / 0.83 h / -20 °C 1.2: NaNO2 / H2O / 2.5 h / -20 °C 2.1: 83 percent / N-bromosuccinimide; benzoylperoxyde / CCl4 / 4 h / Heating 3.1: 83 percent / CaCO3 / H2O / 8 h / Heating View Scheme
Multi-step reaction with 4 steps 1: 88 percent / NaNO2, Br2, 48percent HBr / 5 °C 2: 70 percent / KMnO4 / H2O / Heating 3: 1) NEt3, ethyl chloroformate, 2) LiAlH4 / 1) benzene, rt, 1 h, 2) THF, -78 deg C, 30 min 4: 83 percent / DMSO, N,N'-dicyclohexylcarbodiimide, H3PO4 / 1.5 h / Ambient temperature View Scheme

: 13534-89-9
2,3-dibromopyridine

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: 1.) t-BuLi, i-Pr2NH, 2.) Br2 / 1.) THF, -60 deg C, 2.) -70 deg C, 4 h View Scheme

: 109-04-6
2-bromo-pyridine

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

Conditions

Conditions	Yield
With lithium diisopropyl amide In tetrahydrofuran; water; N,N-dimethyl-formamide
With ammonium chloride; lithium diisopropyl amide In tetrahydrofuran; N-methyl-acetamide

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 35905-85-2
2-bromonicotinic acid

Conditions

Conditions	Yield
With potassium permanganate In water Ambient temperature;	100%
With potassium permanganate In water for 2h; Ambient temperature;	98%

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 131747-54-1
(2-bromopyrid-3-yl)methanol

Conditions

Conditions	Yield
With sodium tetrahydroborate; water In tetrahydrofuran at 20℃; for 2h;	100%
With methanol; sodium tetrahydroborate at 0 - 25℃; for 2h;	90.2%
With sodium tetrahydroborate In methanol at 0 - 20℃; for 1h;	69%

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 100-63-0
phenylhydrazine

: N-(2-bromo-pyridin-3-ylmethylene)-N'-phenyl-hydrazine

Conditions

Conditions	Yield
In 1-methyl-pyrrolidin-2-one at 160℃; for 0.166667h; microwave irradiation;	100%
With acetic acid In ethanol for 2h; Reflux;

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 141-97-9
ethyl acetoacetate

: 109-77-3
malononitrile

: ethyl 6-amino-4-(2-bromo-3-pyridyl)-5-cyano-2-methyl-4H-pyran-3-carboxylate

Conditions

Conditions	Yield
Stage #1: 2-bromopyridine-3-carboxaldehyde; malononitrile With piperidine In methanol at 20℃; Stage #2: ethyl acetoacetate With piperidine In methanol at 20℃; for 0.333333h;	100%

...Expand

: 10365-98-7
3-methoxyphenylboronic acid

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 958219-62-0
2-(3-methoxyphenyl)nicotinaldehyde

Conditions

Conditions	Yield
tetrakis(triphenylphosphine) palladium(0) In 1,2-dimethoxyethane; water for 17h; Heating / reflux;	100%

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 768-60-5
4-methoxyphenylacetylen

: 884501-93-3
2-(4-methoxyphenylethynyl)pyridine-3-carboxaldehyde

Conditions

Conditions	Yield
With copper(l) iodide; triethylamine; bis-triphenylphosphine-palladium(II) chloride at 50℃; for 3h;	99%
Stage #1: 2-bromopyridine-3-carboxaldehyde; 4-methoxyphenylacetylen With trans-bis(triphenylphosphine)palladium dichloride; triethylamine at 20℃; for 0.166667h; Sonogashira Cross-Coupling; Inert atmosphere; Stage #2: With copper(l) iodide at 50℃; for 4h; Sonogashira Cross-Coupling; Inert atmosphere;	61%
With bis(triphenylphosphine)palladium(II) dichloride; triethylamine In acetonitrile for 70h; Sonogashira Cross-Coupling;
Stage #1: 2-bromopyridine-3-carboxaldehyde; 4-methoxyphenylacetylen With trans-bis(triphenylphosphine)palladium dichloride; triethylamine at 20℃; for 0.166667h; Inert atmosphere; Stage #2: With copper(l) iodide at 50℃; Inert atmosphere;

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 104-96-1
4-methylsulfanylaniline

: C13H11BrN2S

Conditions

Conditions	Yield
With magnesium sulfate In tetrahydrofuran at 100℃; for 0.25h; Microwave irradiation;	99%

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 122-51-0
orthoformic acid triethyl ester

: 663170-89-6
2-bromo-3-(diethoxymethyl)pyridine

Conditions

Conditions	Yield
With toluene-4-sulfonic acid In ethanol for 6h; Reflux;	98%
With ammonium chloride In ethanol for 15h; Heating;
With toluene-4-sulfonic acid In ethanol for 6h; Reflux;

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 95-54-5
1,2-diamino-benzene

: 1246929-38-3
2-(2-bromopyridin-3-yl)-1H-benzimidazole

Conditions

Conditions	Yield
With ammonium chloride In methanol at 20℃; for 8h;	98%

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 343338-28-3
(S)-2-methylpropane-2-sulfinamide

: (S,E)-N-[(2-bromopyridin-3-yl)methylene]-tert-butanesulfinamide

Conditions

Conditions	Yield
With titanium(IV) tetraethanolate In tetrahydrofuran at 23℃; for 12h; Inert atmosphere;	98%

: 5720-07-0
4-methoxyphenylboronic acid

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 885949-59-7
2-(4-methoxyphenyl)pyridine-3-carbaldehyde

Conditions

Conditions	Yield
With tetrakis(triphenylphosphine) palladium(0); potassium carbonate In ethanol; water; toluene Inert atmosphere; Reflux;	98%

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 1779-49-3
Methyltriphenylphosphonium bromide

: 932042-98-3
2-bromo-3-vinylpyridine

Conditions

Conditions	Yield
With n-butyllithium In tetrahydrofuran; hexane at 0 - 20℃; for 14h; Wittig reaction;	97%
Stage #1: Methyltriphenylphosphonium bromide With n-butyllithium In tetrahydrofuran at 0 - 20℃; for 0.5h; Stage #2: 2-bromopyridine-3-carboxaldehyde In tetrahydrofuran at 0 - 20℃;	89%
Stage #1: Methyltriphenylphosphonium bromide With n-butyllithium In tetrahydrofuran at 0 - 20℃; for 0.5h; Wittig reaction; Inert atmosphere; Stage #2: 2-bromopyridine-3-carboxaldehyde In tetrahydrofuran at 0 - 20℃; for 72h; Wittig reaction; Inert atmosphere;	89%
Stage #1: Methyltriphenylphosphonium bromide With n-butyllithium In tetrahydrofuran at 0 - 20℃; for 0.5h; Wittig Olefination; Stage #2: 2-bromopyridine-3-carboxaldehyde In tetrahydrofuran at 0 - 20℃; for 72h; Wittig Olefination;	89%

: 2524-49-4
3-butene-1-amine

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: N-[(2-bromopyridin-3-yl)methyl]but-3-en-1-amine

Conditions

Conditions	Yield
Stage #1: 3-butene-1-amine; 2-bromopyridine-3-carboxaldehyde With magnesium sulfate In dichloromethane Stage #2: With sodium tetrahydroborate In methanol	97%

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 536-74-3
phenylacetylene

: 222167-31-9
2-(2-phenylethynyl)pyridine-3-carbaldehyde

Conditions

Conditions	Yield
With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide In triethylamine at 50℃; Sonogashira reaction;	96%
With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine at 50℃; for 5h; Inert atmosphere;	94%
With copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); triethylamine In tetrahydrofuran at 70℃; Inert atmosphere;	93%

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 75-64-9
tert-butylamine

: 536-74-3
phenylacetylene

: N-[(2-phenylethynyl)pyridin-3-ylmethylene]-tert-butylamine

Conditions

Conditions	Yield
Stage #1: 2-bromopyridine-3-carboxaldehyde; phenylacetylene With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide In triethylamine at 50℃; Stage #2: tert-butylamine at 20℃; for 24h; Further stages.;	96%

...Expand

: 75-16-1
methylmagnesium bromide

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 84199-57-5
1-(2′-bromo-3′-pyridyl)ethan-1-ol

Conditions

Conditions	Yield
In tetrahydrofuran at 0 - 5℃;	96%
In diethyl ether; dibutyl ether at -78 - 0℃; Inert atmosphere;	87%
Stage #1: methylmagnesium bromide; 2-bromopyridine-3-carboxaldehyde In tetrahydrofuran at -20 - 0℃; for 0.333333h; Stage #2: With ammonium chloride In tetrahydrofuran; water

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 81290-20-2
(trifluoromethyl)trimethylsilane

: 1092459-51-2
1-(2-bromo-3-pyridinyl)-2,2,2-trifluoroethanol

Conditions

Conditions	Yield
Stage #1: 2-bromopyridine-3-carboxaldehyde; (trifluoromethyl)trimethylsilane In tetrahydrofuran at -70 - 20℃; for 1h; Cooling with methanol-dry ice; Stage #2: With tetrabutyl ammonium fluoride In tetrahydrofuran at 20℃; for 2h; Stage #3: With hydrogenchloride; water In tetrahydrofuran at 20℃; for 1h;	96%

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 57260-71-6
1-t-Butoxycarbonylpiperazine

: tert-butyl 4-[(2-bromopyridin-3-yl)methyl]piperazine-1-carboxylate

Conditions

Conditions	Yield
With sodium tris(acetoxy)borohydride; acetic acid for 16h;	95.99%

: 629-05-0
n-octyne

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 222167-37-5
2-(1-octyn-1-yl)pyridine-3-carboxaldehyde

Conditions

Conditions	Yield
With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide In triethylamine at 50℃; Sonogashira reaction;	95%
With triethylamine; bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide In N,N-dimethyl-formamide for 15h; Ambient temperature;	79%

: 629-05-0
n-octyne

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 75-64-9
tert-butylamine

: N-[2-(1-octyn-1-yl)pyridin-3-ylmethylene]-tert-butylamine

Conditions

Conditions	Yield
Stage #1: n-octyne; 2-bromopyridine-3-carboxaldehyde With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide In triethylamine at 50℃; Stage #2: tert-butylamine at 20℃; for 24h; Further stages.;	95%

...Expand

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 109-76-2
Trimethylenediamine

: 1202518-92-0
2-(2-bromopyridin-3-yl)-1,4,5,6-tetrahydropyrimidine

Conditions

Conditions	Yield
Stage #1: 2-bromopyridine-3-carboxaldehyde; Trimethylenediamine In tert-butyl alcohol at 70℃; for 0.5h; Stage #2: With iodine; potassium carbonate In tert-butyl alcohol at 70℃; for 3h;	95%

: 15016-42-9
2-vinylbenzeneboronic acid

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 1279109-73-7
3-formyl-2-(2-vinylphenyl)pyridine

Conditions

Conditions	Yield
With tetrakis(triphenylphosphine) palladium(0); caesium carbonate In ethanol; toluene at 100℃; for 17h; Suzuki reaction; Inert atmosphere;	95%

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 2-bromo-3-(difluoromethyl)pyridine

Conditions

Conditions	Yield
With diethylamino-sulfur trifluoride In dichloromethane at 25℃; for 4h;	95%
With diethylamino-sulfur trifluoride In dichloromethane at 0 - 20℃; for 12.5h; Inert atmosphere;	33.5%

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 676-58-4
methylmagnesium chloride

: 84199-57-5
1-(2′-bromo-3′-pyridyl)ethan-1-ol

Conditions

Conditions	Yield
In tetrahydrofuran at 0 - 5℃; for 0.5h;	95%
In tetrahydrofuran at 0 - 20℃; Inert atmosphere;

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 75-64-9
tert-butylamine

: (E)-N-((2-bromopyridin-3-yl)methylene)-2-methylpropan-2-amine

Conditions

Conditions	Yield
With water at 25℃;	94%

: C24H20BrNP(1+)*Br(1-)

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 942267-02-9
(Z)-1,2-di(2-bromopyridin-3-yl)ethene

Conditions

Conditions	Yield
With potassium tert-butylate In tetrahydrofuran at 20℃; for 18h; Wittig reaction;	94%

: 120-72-9
indole

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: C22H16BrN3

Conditions

Conditions	Yield
With cadmium sulphide In methanol for 0.25h; Reflux;	94%

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 1099-45-2
ethyl (triphenylphosphoranylidene)acetate

: (E)-ethyl 3-(2-bromopyridin-3-yl)acrylate

Conditions

Conditions	Yield
In dichloromethane at 0 - 20℃; for 8h; Wittig Olefination;	94%
In dichloromethane at 0 - 20℃; for 8h; Wittig Olefination;	94%
In dichloromethane at 0 - 20℃; Wittig Olefination;

: 2,2'-(3,7-di-tert-butyl-9,10-dihydroanthracene-1,5-diyl)bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane)

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: 2,2'-(3,7-di-tert-butyl-9,10-dihydroanthracene-1,5-diyl)dinicotinaldehyde

Conditions

Conditions	Yield
With tris-(dibenzylideneacetone)dipalladium(0); potassium carbonate; tri tert-butylphosphoniumtetrafluoroborate In tetrahydrofuran; water at 80℃; Suzuki-Miyaura Coupling; Sealed tube;	94%

: 4187-87-5
1-Phenyl-2-propyn-1-ol

: 128071-75-0
2-bromopyridine-3-carboxaldehyde

: (Z)-6-(hydroxy(phenyl)methylene)-6,7-dihydro-5H-cyclopenta[b]pyridin-5-one

Conditions

Conditions	Yield
With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; 1,8-diazabicyclo[5.4.0]undec-7-ene In tetrahydrofuran at 20℃; for 4h; Schlenk technique; Inert atmosphere;	94%

2-Bromopyridine-3-carbaldehyde Specification

The 3-Pyridinecarboxaldehyde,2-bromo-, with the CAS registry number 128071-75-0, is also known as 2-Bromo-3-formylpyridine. It belongs to the product categories of Pharmacetical; Aldehydes; Pyridines; Pyridine; Pyridines derivates; Halogenated; Organohalides; Bromopyridines; Halopyridines. This chemical's molecular formula is C₆H₄BrNO and molecular weight is 186.01. What's more, its systematic name is 2-bromopyridine-3-carbaldehyde. It should be sealed and stored in a cool and dry place. Moreover, it should be ensured that the workshop is well ventilated or equipped with exhaust devices. It is used as an organic reagent and a pharmaceutical intermediate.

Physical properties of 3-Pyridinecarboxaldehyde,2-bromo- are: (1)ACD/LogP: 0.99; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 0.99; (4)ACD/LogD (pH 7.4): 0.99; (5)ACD/BCF (pH 5.5): 3.33; (6)ACD/BCF (pH 7.4): 3.33; (7)ACD/KOC (pH 5.5): 82.36; (8)ACD/KOC (pH 7.4): 82.36; (9)#H bond acceptors: 2; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 1; (12)Polar Surface Area: 29.96 Å²; (13)Index of Refraction: 1.619; (14)Molar Refractivity: 38.78 cm³; (15)Molar Volume: 110.5 cm³; (16)Polarizability: 15.37×10^-24cm³; (17)Surface Tension: 52.1 dyne/cm; (18)Density: 1.683 g/cm³; (19)Flash Point: 115.7 °C; (20)Enthalpy of Vaporization: 50.58 kJ/mol; (21)Boiling Point: 267.7 °C at 760 mmHg; (22)Vapour Pressure: 0.00802 mmHg at 25°C.

When you are using this chemical, please be cautious about it as the following:
This chemical is harmful if swallowed. It is irritating to eyes and may cause sensitisation by skin contact. In case of contact with eyes, you should rinse immediately with plenty of water and seek medical advice. When using it, you need wear suitable protective clothing and gloves.

You can still convert the following datas into molecular structure:
(1)SMILES: O=Cc1cccnc1Br
(2)Std. InChI: InChI=1S/C6H4BrNO/c7-6-5(4-9)2-1-3-8-6/h1-4H
(3)Std. InChIKey: GNFWMEFWZWXLIN-UHFFFAOYSA-N

Product Name

2-BROMO-3-FORMYLPYRIDINE

Synthetic route

2-Bromopyridine-3-carbaldehyde Specification

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