Pyrrole-3-carboxaldehyde supplier

Name
Pyrrole-3-carboxaldehyde
EINECS
CAS No. 7126-39-8
Article Data46
CAS DataBase
Density 1.197 g/cm³
Solubility
Melting Point
Formula C₅H₅NO
Boiling Point 238.3 °C at 760 mmHg
Molecular Weight 95.1008
Flash Point 103.9 °C
Transport Information
Appearance
Safety
Risk Codes
Molecular Structure
Hazard Symbols Xi
Synonyms Pyrrole-3-carboxaldehyde(7CI,8CI);3-Formylpyrrole;1H-Pyrrole-3-carboxaldehyde 95%;3-Pyrrolecarboxaldehyde;pyrrole-3-carboxaldehyde;pyrrole-3-carbaldehyde;AC-776/25122024;AC1LD0DZ;CID640308;ZINC02581109;AC-4315;TL80073582;
PSA 32.86000
LogP 0.82720

Synthetic route

: 87630-35-1
N-triisopropylsilylpyrrole

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

: 7126-39-8
pyrrole-3-carboxaldehyde

Conditions

Conditions	Yield
Stage #1: N,N-dimethyl-formamide With phosgene In dichloromethane at 0℃; for 0.5h; Stage #2: N-triisopropylsilylpyrrole In dichloromethane for 0.5h; Reflux; Stage #3: With sodium hydroxide at 20℃; for 12h;	98%
Stage #1: N,N-dimethyl-formamide With oxalyl dichloride In dichloromethane at 0℃; for 0.5h; Inert atmosphere; Stage #2: N-triisopropylsilylpyrrole In dichloromethane at 50℃; for 0.5h; Inert atmosphere; Stage #3: With sodium hydroxide at 20℃; Inert atmosphere;	85%
Stage #1: N,N-dimethyl-formamide With trichlorophosphate at 0 - 5℃; for 1.5h; Vilsmeier-Haack Formylation; Stage #2: N-triisopropylsilylpyrrole In dichloromethane for 2h;	71.9%

: 90971-76-9
1-(triisopropylsilyl)-1H-pyrrole-3-carbaldehyde

: 7126-39-8
pyrrole-3-carboxaldehyde

Conditions

Conditions	Yield
With tetrabutyl ammonium fluoride	86%
With tetrabutyl ammonium fluoride In tetrahydrofuran for 0.0833333h; Ambient temperature;	86%
With sodium hydroxide for 4h; Inert atmosphere;

: 7126-53-6
4-formyl-1H-pyrrole-2-carboxylic acid

A: 7126-39-8
pyrrole-3-carboxaldehyde

B: 124-38-9
carbon dioxide

Conditions

Conditions	Yield
With copper chromite In quinoline at 185℃; for 0.2h;	A 76% B n/a

: 87630-35-1
N-triisopropylsilylpyrrole

: 3724-43-4, 149409-22-3
Vilsmeier reagent

: 7126-39-8
pyrrole-3-carboxaldehyde

Conditions

Conditions	Yield
With sodium hydroxide	72%

: 35302-95-5
2,4,5-triiodo-3-formylpyrrole

: 7126-39-8
pyrrole-3-carboxaldehyde

Conditions

Conditions	Yield
With hydrogen; sodium acetate; palladium on activated charcoal In ethanol under 2585.7 Torr; for 2h;	70%

: 117067-97-7
isopropylidene-(1H-pyrrol-3-yl)-ammonium chloride

: 7126-39-8
pyrrole-3-carboxaldehyde

Conditions

Conditions	Yield
With sodium hydroxide for 4h; Ambient temperature;	69%
With sodium hydroxide In water at 20℃; for 2h;	37.6%
With sodium hydroxide; water at 20℃; for 4h;

: 934961-85-0
(E)-1,1-difluoro-4-ethoxy-2-(aminomethyl)-3-buten-2-ol

: 7126-39-8
pyrrole-3-carboxaldehyde

Conditions

Conditions	Yield
With hydrogenchloride In water; acetonitrile at 20℃; for 24h;	48%

: 3724-43-4, 149409-22-3
Vilsmeier reagent

: 7126-39-8
pyrrole-3-carboxaldehyde

Conditions

Conditions	Yield
Stage #1: pyrrole With sodium hydride In tetrahydrofuran at 0℃; for 1.5h; Stage #2: With triisopropylsilyl chloride In tetrahydrofuran at 0 - 10℃; for 1.5h; Stage #3: Vilsmeier reagent With sodium hydroxide; water more than 3 stages;	38%

: 1-(trisopropylsilyl)pyrrole

: 3724-43-4, 149409-22-3
Vilsmeier reagent

: 7126-39-8
pyrrole-3-carboxaldehyde

Conditions

Conditions	Yield
Stage #1: 1-(trisopropylsilyl)pyrrole; Vilsmeier reagent In dichloromethane at 0℃; Vilsmeier formylation; Reflux; Stage #2: With water; sodium hydroxide at 20℃; for 2h;	38%

: 1003-29-8
2-pyrrole aldehyde

: 7126-39-8
pyrrole-3-carboxaldehyde

Conditions

Conditions	Yield
With trifluorormethanesulfonic acid	22%
With trifluorormethanesulfonic acid In 1,2-dichloro-ethane for 21h; Heating;	3 g

: 1236203-44-3
N-(hydroxy-2' ethyl)amino-3 propenoate d'ethyle

A: 24771-28-6
pyrrole carboxaldehyde

B: 1003-29-8
2-pyrrole aldehyde

C: 7126-39-8
pyrrole-3-carboxaldehyde

Conditions

Conditions	Yield
In tetrahydrofuran at 400℃; sealed tube;	A n/a B 16% C 19%
In tetrahydrofuran at 400℃; sealed tube;	A n/a B n/a C 19%

...Expand

: 111469-20-6
3-<(2-tosylhydrazino)carbonyl>pyrrole

: 7126-39-8
pyrrole-3-carboxaldehyde

Conditions

Conditions	Yield
With sodium carbonate In ethylene glycol at 170℃; for 0.0833333h;	15%

: 1078691-95-8
(+)-D-glucosamine hydrochloride

: malondialdehyde sodium salt

A: 7126-39-8
pyrrole-3-carboxaldehyde

B: 128766-31-4
5-(D-arabino-tetritol-1-yl)-3-pyrrolecarbaldehyde

C: 128766-36-9
5-(β-D-erythrofuranosyl)-3-pyrrolecarbaldehyde

D: 128766-30-3
5-(α-D-erythrofuranosyl)-3-pyrrolecarbaldehyde

Conditions

Conditions	Yield
Yield given. Multistep reaction. Yields of byproduct given;

...Expand

: 1078691-95-8
(+)-D-glucosamine hydrochloride

: malondialdehyde sodium salt

A: 7126-39-8
pyrrole-3-carboxaldehyde

B: 128766-31-4
5-(D-arabino-tetritol-1-yl)-3-pyrrolecarbaldehyde

C: 128766-30-3
5-(α-D-erythrofuranosyl)-3-pyrrolecarbaldehyde

Conditions

Conditions	Yield
With sodium carbonate 1) H2O, room temp., 24h, 2) 90 deg C, 1h; Yield given. Multistep reaction. Yields of byproduct given;

...Expand

: 128766-23-4
2-deoxy-2-<(3'-oxo-1'-propen-1'-yl)amino>-α-D-glucopyranose

A: 7126-39-8
pyrrole-3-carboxaldehyde

B: 128766-31-4
5-(D-arabino-tetritol-1-yl)-3-pyrrolecarbaldehyde

C: 128766-36-9
5-(β-D-erythrofuranosyl)-3-pyrrolecarbaldehyde

D: 128766-30-3
5-(α-D-erythrofuranosyl)-3-pyrrolecarbaldehyde

Conditions

Conditions	Yield
With sodium carbonate In water-d2 at 90℃; for 1h; Yield given. Yields of byproduct given;

...Expand

: 87630-35-1
N-triisopropylsilylpyrrole

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

A: 1003-29-8
2-pyrrole aldehyde

B: 7126-39-8
pyrrole-3-carboxaldehyde

Conditions

Conditions	Yield
With sodium hydroxide; pyrophosphoryl chloride 1) acetonitrile, 20 deg C, 2 h; Yield given. Multistep reaction. Yields of byproduct given;

...Expand

: 87630-35-1
N-triisopropylsilylpyrrole

: 93-61-8
N-methyl-N-phenylformamide

A: 1003-29-8
2-pyrrole aldehyde

B: 7126-39-8
pyrrole-3-carboxaldehyde

Conditions

Conditions	Yield
With sodium hydroxide; pyrophosphoryl chloride 1) acetonitrile, 20 deg C, 2 h; Yield given. Multistep reaction. Yields of byproduct given;
Yield given. Multistep reaction. Yields of byproduct given;

...Expand

: pyrrole-1,3-dicarbaldehyde

: 7126-39-8
pyrrole-3-carboxaldehyde

Conditions

Conditions	Yield
With sodium hydroxide In acetonitrile at 20℃; for 0.5h;

: 405219-05-8
1-diethoxymethyl-1H-pyrrole-3-carbaldehyde

: 7126-39-8
pyrrole-3-carboxaldehyde

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: TFA / acetonitrile / 1 h / 20 °C 2: aq. NaOH / acetonitrile / 0.5 h / 20 °C View Scheme

: 2703-17-5
methyl 1H-pyrrole-3-carboxylate

: 7126-39-8
pyrrole-3-carboxaldehyde

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: hydrazine / 2 h / Heating 2: pyridine / 0.5 h / 20 °C 3: 15 percent / sodium carbonate / ethane-1,2-diol / 0.08 h / 170 °C View Scheme

: 50561-16-5
pyrrole-3-carboxylic acid hydrazide

: 7126-39-8
pyrrole-3-carboxaldehyde

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: pyridine / 0.5 h / 20 °C 2: 15 percent / sodium carbonate / ethane-1,2-diol / 0.08 h / 170 °C View Scheme

: 931-03-3
1H-pyrrole-3-carboxylic acid

: 7126-39-8
pyrrole-3-carboxaldehyde

Conditions

Conditions	Yield
Multi-step reaction with 3 steps 1: thionyl chloride / 1 h / 0 - 130 °C / Inert atmosphere; Microwave irradiation 2: diisobutylaluminium hydride / dichloromethane; toluene / 0.5 h / -78 °C / Inert atmosphere 3: manganese(IV) oxide / methanol / 20 °C View Scheme

: 37964-17-3
pyrrole-3-carboxylic acid ethyl ester

: 7126-39-8
pyrrole-3-carboxaldehyde

Conditions

Conditions	Yield
Multi-step reaction with 2 steps 1: diisobutylaluminium hydride / dichloromethane; toluene / 0.5 h / -78 °C / Inert atmosphere 2: manganese(IV) oxide / methanol / 20 °C View Scheme

: 3-hydroxymethyl-1H-pyrrole

: 7126-39-8
pyrrole-3-carboxaldehyde

Conditions

Conditions	Yield
With manganese(IV) oxide In methanol at 20℃;

: 109-97-7
pyrrole

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

: 7126-39-8
pyrrole-3-carboxaldehyde

Conditions

Conditions	Yield
Stage #1: pyrrole With sodium hydride In tetrahydrofuran at -10℃; for 1.5h; Stage #2: With triisopropylsilyl chloride In tetrahydrofuran at 20℃; Stage #3: N,N-dimethyl-formamide With oxalyl dichloride In dichloromethane at -10℃; for 4h;

: 7126-39-8
pyrrole-3-carboxaldehyde

: 75-09-2
dichloromethane

: 81263-90-3
1,1'-methylenebis(1H-pyrrole-2-carboxaldehyde)

Conditions

Conditions	Yield
With sodium hydroxide; tetra-(n-butyl)ammonium iodide In dichloromethane for 5h;	98%

: 7126-39-8
pyrrole-3-carboxaldehyde

: 3416-74-8
1-chloro-4-nonyne

: 1-(non-4-yn-1-yl)-1H-pyrrole-3-carbaldehyde

Conditions

Conditions	Yield
With caesium carbonate; sodium iodide In acetonitrile at 80℃; for 16h; Sealed tube;	98%

: 495-69-2
Hippuric Acid

: 7126-39-8
pyrrole-3-carboxaldehyde

: (Z)-4-((1H-pyrrol-3-yl)methylene)-2-phenyloxazol-5(4H)-one

Conditions

Conditions	Yield
Stage #1: Hippuric Acid With triethylamine sulfate at 80℃; for 0.0833333h; Green chemistry; Stage #2: pyrrole-3-carboxaldehyde at 100℃; for 0.333333h; Reagent/catalyst; Green chemistry; stereoselective reaction;	97%
Stage #1: Hippuric Acid; pyrrole-3-carboxaldehyde With sodium acetate; acetic anhydride for 2h; Heating; Stage #2: In ethanol at 20℃; for 18h; Stage #3: With PPA at 80 - 90℃; for 2h;	60%

: 7126-39-8
pyrrole-3-carboxaldehyde

: 74-89-5
methylamine

: 3-Methyliminomethyl pyrrole

Conditions

Conditions	Yield
In acetonitrile Ambient temperature;	95%

: 7126-39-8
pyrrole-3-carboxaldehyde

: 114192-88-0, 136964-14-2, 3108-34-7
4,4,4‐trifluoro‐1‐phenyl‐2‐buten‐1‐one

: 1-(1,1,1-trifluoro-4-oxo-4-phenylbutan-2-yl)-1H-pyrrole-3-carbaldehyde

Conditions

Conditions	Yield
With (2S)-2-{diphenyl[(trimethylsilyl)oxy]methyl}pyrrolidine; benzoic acid In toluene at 40℃; for 24h;	95%

: 7126-39-8
pyrrole-3-carboxaldehyde

: 32597-35-6
pyrrole-3-carboxaldehyde oxime

Conditions

Conditions	Yield
With hydroxylamine hydrochloride; potassium carbonate In water for 0.5h; Heating;	94%

: 7126-39-8
pyrrole-3-carboxaldehyde

: 24424-99-5
di-tert-butyl dicarbonate

: 209216-57-9
tert-butyl 3-formylpyrrole-1-carboxylate

Conditions

Conditions	Yield
With dmap; N-ethyl-N,N-diisopropylamine In dichloromethane 0 deg C, 3 h then r.t., 1 h;	93%
In acetonitrile at 25℃; for 24h;

: 7126-39-8
pyrrole-3-carboxaldehyde

: 122-51-0
orthoformic acid triethyl ester

: 405219-05-8
1-diethoxymethyl-1H-pyrrole-3-carbaldehyde

Conditions

Conditions	Yield
for 24h; Heating;	92%

: 7126-39-8
pyrrole-3-carboxaldehyde

: 75-31-0
isopropylamine

: 3-Isopropyliminomethyl pyrrole

Conditions

Conditions	Yield
In acetonitrile Ambient temperature;	91%

: 7126-39-8
pyrrole-3-carboxaldehyde

: C14H9F3O

: 1-(1,1,1-trifluoro-4-(naphthalen-2-yl)-4-oxobutan-2-yl)-1H-pyrrole-3-carbaldehyde

Conditions

Conditions	Yield
With (2S)-2-{diphenyl[(trimethylsilyl)oxy]methyl}pyrrolidine; benzoic acid In toluene at 40℃; for 24h;	91%

: 7126-39-8
pyrrole-3-carboxaldehyde

: 98-09-9
benzenesulfonyl chloride

: 88075-95-0
1-(phenylsulfonyl)-1H-pyrrole-3-carbaldehyde

Conditions

Conditions	Yield
With tetrabutylammomium bromide; sodium hydroxide In dichloromethane; water at 15℃; for 24h;	90.95%

: 55315-56-5
2-(3-methylbutoxy)-1,3-benzodithiole

: 7126-39-8
pyrrole-3-carboxaldehyde

: 153850-69-2
2,5-bis(1,3-benzodithiol-2-yl)-3-formylpyrrole

Conditions

Conditions	Yield
With acetic acid at 70℃; for 2h;	90%

: 7126-39-8
pyrrole-3-carboxaldehyde

: 106-96-7
propargyl bromide

: 1-(2-propynyl)-1H-pyrrole-3-carboxaldehyde

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide Inert atmosphere;	90%
In tetrahydrofuran

: 7126-39-8
pyrrole-3-carboxaldehyde

: C10H6ClF3O

: 1-(4-(3-chlorophenyl)-1,1,1-trifluoro-4-oxobutan-2-yl)-1H-pyrrole-3-carbaldehyde

Conditions

Conditions	Yield
With (2S)-2-{diphenyl[(trimethylsilyl)oxy]methyl}pyrrolidine; benzoic acid In toluene at 40℃; for 24h;	90%

: 7126-39-8
pyrrole-3-carboxaldehyde

: 16695-14-0
Malonic acid monomethyl ester

: 352538-45-5
(Z)-3-(1H-Pyrrol-3-yl)-acrylic acid methyl ester

Conditions

Conditions	Yield
With piperidine In pyridine at 65℃; for 21h;	89%

: 7126-39-8
pyrrole-3-carboxaldehyde

: 1099-45-2
ethyl (triphenylphosphoranylidene)acetate

: ethyl (E)-3-(1H-pyrrol-3-yl)prop-2-eneacetate

Conditions

Conditions	Yield
In ethanol at 80℃; Wittig Olefination;	89%

: 7126-39-8
pyrrole-3-carboxaldehyde

: 98-59-9
p-toluenesulfonyl chloride

: 117954-70-8
3-formyl-1-<(4-methylphenyl)sulfonyl>pyrrole

Conditions

Conditions	Yield
With sodium hydroxide; tetra(n-butyl)ammonium hydrogensulfate In dichloromethane for 0.25h; cooled;	88%
Stage #1: pyrrole-3-carboxaldehyde With sodium hydroxide In dichloromethane at 0℃; for 0.166667h; Stage #2: p-toluenesulfonyl chloride In dichloromethane at 0 - 20℃; for 19h;	88%
Stage #1: pyrrole-3-carboxaldehyde With sodium hydride In tetrahydrofuran; mineral oil at 0℃; Inert atmosphere; Stage #2: p-toluenesulfonyl chloride In tetrahydrofuran; mineral oil at 20℃; for 4h; Inert atmosphere;	77%
With dmap; triethylamine In dichloromethane at 20℃; for 12h;
With triethylamine In dichloromethane at 20℃;

: 7126-39-8
pyrrole-3-carboxaldehyde

: 100-39-0
benzyl bromide

: 30186-48-2
1-benzyl-1H-pyrrole-3-carbaldehyde

Conditions

Conditions	Yield
With sodium hydroxide; tetrabutylammomium bromide In dichloromethane at 0 - 20℃;	88%

: 7126-39-8
pyrrole-3-carboxaldehyde

: 33797-51-2
eschenmoser's salt

: C8H12N2O

Conditions

Conditions	Yield
In acetonitrile at 60℃; Mannich Aminomethylation;	87%

: 7126-39-8
pyrrole-3-carboxaldehyde

: C14H23O8PS

: C15H17NO5S

Conditions

Conditions	Yield
Stage #1: C14H23O8PS With sodium hydride In tetrahydrofuran at 0℃; for 0.25h; Wittig-Horner Reaction; Inert atmosphere; Stage #2: pyrrole-3-carboxaldehyde In tetrahydrofuran for 1h; Wittig-Horner Reaction; Inert atmosphere;	86.7%

: 7126-39-8
pyrrole-3-carboxaldehyde

: 4712-55-4
diphenyl hydrogen phosphite

: 101-77-9
4,4'-diamino diphenyl methane

: tetraphenyl{[(methylenebis(4,1-phenylene))bis(azanediyl)]bis[(3-pyrrole)methylene]}diphosphonate

Conditions

Conditions	Yield
at 80℃; for 4h; Kabachnik-Fields Reaction; Green chemistry;	86%

...Expand

: 7126-39-8
pyrrole-3-carboxaldehyde

: 74-88-4
methyl iodide

: 36929-60-9
3-formyl-1-methylpyrrole

Conditions

Conditions	Yield
With 16-crown-6; potassium tert-butylate In cyclohexane; dimethyl sulfoxide	85%
Stage #1: pyrrole-3-carboxaldehyde With sodium hydride In N,N-dimethyl-formamide; mineral oil at 0 - 20℃; for 0.5h; Stage #2: methyl iodide In N,N-dimethyl-formamide; mineral oil at 0 - 20℃; for 1h;	35%
Stage #1: pyrrole-3-carboxaldehyde With sodium hydride In N,N-dimethyl-formamide at 0 - 20℃; for 0.5h; Stage #2: methyl iodide In N,N-dimethyl-formamide at 20℃; for 1h;	35%
With sodium hydride In tetrahydrofuran for 4.25h; Inert atmosphere;	610 mg

: 7126-39-8
pyrrole-3-carboxaldehyde

: 106-95-6
allyl bromide

: 1-allyl-1H-pyrrole-3-carboxaldehyde

Conditions

Conditions	Yield
Stage #1: pyrrole-3-carboxaldehyde With potassium hydroxide In dimethyl sulfoxide at 20℃; for 0.833333h; Stage #2: allyl bromide In dimethyl sulfoxide at 20℃; for 4h;	84%

: 7126-39-8
pyrrole-3-carboxaldehyde

: 292638-85-8
acrylic acid methyl ester

: methyl 3-(3-formyl-1H-pyrrol-1-yl)propanoate

Conditions

Conditions	Yield
With 1,8-diazabicyclo[5.4.0]undec-7-ene In acetonitrile Reflux;	84%

: 1123-49-5
3,5-dimethyl-4-nitroisoxazole

: 7126-39-8
pyrrole-3-carboxaldehyde

: 3-methyl-4-nitro-5-[2-(1H-pyrrol-2-yl)vinyl]isoxazole

Conditions

Conditions	Yield
With piperidine In ethanol at 65℃; for 2h;	83%

: 95-20-5
2-methyl-1H-indole

: 7126-39-8
pyrrole-3-carboxaldehyde

: C23H21N3

Conditions

Conditions	Yield
With diammonium phosphate at 80℃; for 3.5h;	82%

: 7126-39-8
pyrrole-3-carboxaldehyde

: 2646-31-3
4-(p-bromophenyl)thiosemicarbazide

: (E)-2-((1H-pyrrol-3-yl)methylene)-N-(4-bromophenyl)hydrazine-1-carbothioamide

Conditions

Conditions	Yield
With acetic acid In methanol for 2h; Reflux;	82%

: 7126-39-8
pyrrole-3-carboxaldehyde

: 4336-70-3
(cyanomethyl)triphenylphosphonium chloride

: 3-(1H-pyrrol-3-yl)-acrylonitrile

Conditions

Conditions	Yield
With 1,8-diazabicyclo[5.4.0]undec-7-ene In toluene at 115℃; for 1.5h;	80.5%
With 1,8-diazabicyclo[5.4.0]undec-7-ene In toluene for 1h; Wittig Olefination; Reflux;	67 g

Pyrrole-3-carboxaldehyde Specification

The Pyrrole-3-carboxaldehyde with CAS registry number of 7126-39-8 is also known as 3-Pyrrolecarboxaldehyde. The IUPAC name is 1H-pyrrole-3-carbaldehyde. It belongs to product categories of Pharmaceutial intermediates; Aldehydes; Pyrroles & Indoles; Pyrroles & Indoles. In addition, the formula is C₅H₅NO and the molecular weight is 95.10. This chemical may cause inflammation to the skin or other mucous membranes.

Physical properties about Pyrrole-3-carboxaldehyde are: (1)ACD/LogP: 0.17; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 0.17; (4)ACD/LogD (pH 7.4): 0.17; (5)ACD/BCF (pH 5.5): 1; (6)ACD/BCF (pH 7.4): 1; (7)ACD/KOC (pH 5.5): 29.54; (8)ACD/KOC (pH 7.4): 29.54; (9)#H bond acceptors: 2; (10)#H bond donors: 1; (11)#Freely Rotating Bonds: 1; (12)Polar Surface Area: 22Å²; (13)Index of Refraction: 1.607; (14)Molar Refractivity: 27.43 cm³; (15)Molar Volume: 79.4 cm³; (16)Polarizability: 10.87×10^-24cm³; (17)Surface Tension: 50.7 dyne/cm; (18)Density: 1.197 g/cm³; (19)Flash Point: 103.9 °C; (20)Enthalpy of Vaporization: 47.52 kJ/mol; (21)Boiling Point: 238.3 °C at 760 mmHg; (22)Vapour Pressure: 0.0426 mmHg at 25 °C.

You can still convert the following datas into molecular structure:
1. SMILES: O=Cc1ccnc1
2. InChI: InChI=1/C5H5NO/c7-4-5-1-2-6-3-5/h1-4,6H
3. InChIKey: CHNYVNOFAWYUEG-UHFFFAOYAQ
4. Std. InChI: InChI=1S/C5H5NO/c7-4-5-1-2-6-3-5/h1-4,6H
5. Std. InChIKey: CHNYVNOFAWYUEG-UHFFFAOYSA-N

Product Name

Pyrrole-3-carboxaldehyde

Synthetic route

Pyrrole-3-carboxaldehyde Specification

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