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2-METHYL-1H-PYRROLE-3-CARBOXYLIC ACID

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2-METHYL-1H-PYRROLE-3-CARBOXYLIC ACID Basic information

Product Name:
2-METHYL-1H-PYRROLE-3-CARBOXYLIC ACID
Synonyms:
  • 2-METHYL-1H-PYRROLE-3-CARBOXYLIC ACID
  • 2-Methylpyrrole-3-carboxylic acid
  • 1H-Pyrrole-3-carboxylic acid, 2-Methyl-
  • 2-Methyl-1H-Pyrrole-3-Carboxylic Acid(WX614100)
  • 2-Methyl-3-pyrrolecarboxylic acid
CAS:
37102-48-0
MF:
C6H7NO2
MW:
125.13
Mol File:
37102-48-0.mol
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2-METHYL-1H-PYRROLE-3-CARBOXYLIC ACID Chemical Properties

Melting point:
178-179℃
Boiling point:
322.4±22.0 °C(Predicted)
Density 
1.295
storage temp. 
Sealed in dry,Room Temperature
form 
solid
pka
5.60±0.50(Predicted)
Appearance
Light brown to brown Solid
InChI
InChI=1S/C6H7NO2/c1-4-5(6(8)9)2-3-7-4/h2-3,7H,1H3,(H,8,9)
InChIKey
YBJBJOLFTYIFKP-UHFFFAOYSA-N
SMILES
N1C=CC(C(O)=O)=C1C
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26
WGK Germany 
3
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2-METHYL-1H-PYRROLE-3-CARBOXYLIC ACID Usage And Synthesis

Uses

2-Methyl-1H-Pyrrole-3-carboxylic acid was examined for its inhibitory properties of BET bromodomains. 2-Methyl-1H-Pyrrole-3-carboxylic acid is also patented as a plant-growth regulator.

Synthesis

936-12-9

37102-48-0

Example 149a Synthesis of 2-methyl-1H-pyrrole-3-carboxylic acid: an aqueous solution (20 mL) of lithium hydroxide (1.563 g, 65.3 mmol) was added to a solution of dioxane (20 mL) containing ethyl 2-methyl-1H-pyrrole-3-carboxylate (2.0 g, 13.06 mmol). The reaction mixture was heated under reflux conditions for 4 hours. Upon completion of the reaction, the mixture was cooled to room temperature and subsequently extracted by partitioning with ethyl acetate and 1 M hydrochloric acid. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to afford the target compound 2-methyl-1H-pyrrole-3-carboxylic acid (1.513 g, 93% yield).

References

[1] Patent: US2014/275079, 2014, A1. Location in patent: Paragraph 0604
[2] Organic and Biomolecular Chemistry, 2015, vol. 13, # 29, p. 7911 - 7914
[3] Bioorganic and Medicinal Chemistry Letters, 2017, vol. 27, # 10, p. 2225 - 2233
[4] Chemische Berichte, 1911, vol. 44, p. 490
[5] Chemische Berichte, 1918, vol. 51, p. 569

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