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METHYL 3-AMINO-5-METHYLTHIOPHENE-2-CARBOXYLATE

CAS No.
76575-71-8
Chemical Name:
METHYL 3-AMINO-5-METHYLTHIOPHENE-2-CARBOXYLATE
Synonyms
Methyl 3-aMino-5-Methylthiophen-2-carboxylate;METHYL 3-AMINO-5-METHYLTHIOPHENE-2-CARBOXYLATE;Methyl 3-amino-5-methylthiophene-2-carboxylate 95+%;3-AMINO-5-METHYLTHIOPHENE-2-CARBOXYLIC ACID, MET. ESTER;5-Methyl-3-aMinothiophene-2-carboxylic acid Methyl ester;Methyl 3-amino-5-methylthiophene-2-carboxylic acid ester;3-Amino-5-methyl-2-thiophenecarboxylic acid methyl ester;3-AMINO-5-METHYL-THIOPHENE-2-CARBOXYLIC ACID METHYL ESTER;2-Thiophenecarboxylic acid, 3-amino-5-methyl-, methyl ester;Methyl 3-Amino-5-methylthiophene-2-carboxylate, CAS 76575-71-8
CBNumber:
CB6290133
Molecular Formula:
C7H9NO2S
Molecular Weight:
171.22
MDL Number:
MFCD00130095
MOL File:
76575-71-8.mol
MSDS File:
SDS
Last updated:2025-08-08 17:45:00

METHYL 3-AMINO-5-METHYLTHIOPHENE-2-CARBOXYLATE Properties

Melting point 84-85℃ (methanol )
Boiling point 319.2±37.0 °C(Predicted)
Density 1.264±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
pka 2.08±0.10(Predicted)
form Solid
Appearance Light yellow to light brown Solid
Water Solubility Slightly soluble in water.
InChI InChI=1S/C7H9NO2S/c1-4-3-5(8)6(11-4)7(9)10-2/h3H,8H2,1-2H3
InChIKey FVKMOPIFLCMZMI-UHFFFAOYSA-N
SMILES C1(C(OC)=O)SC(C)=CC=1N

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P280a-P304+P340-P305+P351+P338-P405-P501a
Hazard Codes  Xi
HazardClass  IRRITANT
HS Code  2921490090
NFPA 704
0
2 0

METHYL 3-AMINO-5-METHYLTHIOPHENE-2-CARBOXYLATE price More Price(34)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC M328535 Methyl3-amino-5-methylthiophene-2-carboxylate 76575-71-8 100mg $75 2021-12-16 Buy
TRC M328535 Methyl3-amino-5-methylthiophene-2-carboxylate 76575-71-8 500mg $255 2021-12-16 Buy
TRC M328535 Methyl3-amino-5-methylthiophene-2-carboxylate 76575-71-8 1g $385 2021-12-16 Buy
Apolloscientific OR318100 Methyl3-amino-5-methylthiophene-2-carboxylate 97% 76575-71-8 10g $385 2021-12-16 Buy
SynQuest Laboratories 8H66-1-4X Methyl 3-amino-5-methylthiophene-2-carboxylate 76575-71-8 1g $349 2021-12-16 Buy
Product number Packaging Price Buy
M328535 100mg $75 Buy
M328535 500mg $255 Buy
M328535 1g $385 Buy
OR318100 10g $385 Buy
8H66-1-4X 1g $349 Buy

METHYL 3-AMINO-5-METHYLTHIOPHENE-2-CARBOXYLATE Chemical Properties,Uses,Production

Uses

Methyl 3-amino-5-methylthiophene-2-carboxylate is employed as a intermediate for pharmaceutical and chemical research.

Synthesis

Crotononitrile (pract)

4786-20-3

Methyl thioglycolate

2365-48-2

METHYL 3-AMINO-5-METHYLTHIOPHENE-2-CARBOXYLATE

76575-71-8

General procedure for the synthesis of methyl 3-amino-5-methylthiophene-2-carboxylate from 2-butenenitrile and methyl mercaptoacetate: a mixture of cis- and trans-2-butenenitrile (298.00 g, 4.44 mol) was mixed with pyridine (61.49 g, 0.78 mol) and the resulting mixture was cooled to 0 °C. Chlorine gas (314.92 g, 4.44 mol) was passed at a rate of 60-65 g/h while maintaining the internal temperature at 10-13 °C. After addition, the reaction mixture was slowly warmed to room temperature and stirred overnight. The resulting oil was dissolved in dichloromethane (1.5 L) to allow the solution to pass through a silica gel column for initial purification. The filtrate was concentrated under vacuum to give the complex reaction mixture (508.61 g) as a brown oily substance. This oily substance (493.80 g) was mixed with methyl mercaptoacetate (422.77 g, 3.98 mol), and the resulting solution was slowly (1.5 h) added dropwise to a methanol (2.2 L) slurry of potassium carbonate (1651 g, 11.95 mol) at 100 °C. The final slurry was allowed to warm to room temperature and stirred at ambient temperature for 5 hours. The solid salt was filtered out and washed with methanol (2L). Combine the organic solutions and evaporate the solvent. The residue was redissolved in ethyl acetate (3L) and subjected to secondary purification via silica gel column. The silica gel column was washed with additional ethyl acetate (2L). All organic phases were combined and the solvent was evaporated under vacuum to give a brown oil (627 g). The mixture was vacuum distilled at 6 mmHg under reduced pressure. The fraction collected at 138°C was crystallized in a receiving flask (303.07 g). The target product methyl 3-amino-5-methylthiophene-2-carboxylate (179.00 g, 26%) was obtained as white crystals by recrystallization from methanol. The structure of the product was confirmed by 1H NMR (CDCl3, 400 MHz) and 13C NMR (CDCl3, 100 MHz).

References

[1] Patent: WO2007/23382, 2007, A2. Location in patent: Page/Page column 64

4786-20-3
2365-48-2
76575-71-8
Synthesis of METHYL 3-AMINO-5-METHYLTHIOPHENE-2-CARBOXYLATE from Crotononitrile (pract) and Methyl thioglycolate
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METHYL 3-AMINO-5-METHYLTHIOPHENE-2-CARBOXYLATE Spectrum

3-AMINO-5-METHYL-THIOPHENE-2-CARBOXYLIC ACID METHYL ESTER METHYL 3-AMINO-5-METHYLTHIOPHENE-2-CARBOXYLATE Methyl 3-amino-5-methylthiophene-2-carboxylate 95+% 3-Amino-5-methyl-2-thiophenecarboxylic acid methyl ester Methyl 3-aMino-5-Methylthiophen-2-carboxylate 3-AMINO-5-METHYLTHIOPHENE-2-CARBOXYLIC ACID, MET. ESTER 5-Methyl-3-aMinothiophene-2-carboxylic acid Methyl ester 2-Thiophenecarboxylic acid, 3-amino-5-methyl-, methyl ester Methyl 3-amino-5-methylthiophene-2-carboxylic acid ester Methyl 3-Amino-5-methylthiophene-2-carboxylate, CAS 76575-71-8 76575-71-8