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Methyl 3-amino-2-thiophenecarboxylate

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Methyl 3-amino-2-thiophenecarboxylate Basic information

Product Name:
Methyl 3-amino-2-thiophenecarboxylate
Synonyms:
  • AMino-2-thiophenecarboxylate
  • AMino thiophene - 2-3 - carboxylic acid Methyl ester
  • Methyl3-aMino-2-thiophenecarbo
  • RARECHEM AM UC 0123
  • 3-amino-2-thiophenecarboxylicacimethylester
  • ina-5545-2
  • Methyl3-amino-2-thenoate
  • 3-AMINO-2-METHOXYCARBONYLTHIOPHENE
CAS:
22288-78-4
MF:
C6H7NO2S
MW:
157.19
EINECS:
244-895-8
Product Categories:
  • API intermediates
  • Thiophenes & Benzothiophenes
  • Sulphur Derivatives
  • INTERMEDIATESOFTENOXICAM
  • Esters
  • Pharmaceutical intermediate
  • Amino Acids and Derivatives
  • Heterocycles
  • Thiophenes & Benzothiophenes
  • Thiophene&Benzothiophene
  • Building Blocks
  • Heterocyclic Building Blocks
  • Thiophenes
  • Pyridines
  • bc0001
Mol File:
22288-78-4.mol
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Methyl 3-amino-2-thiophenecarboxylate Chemical Properties

Melting point:
62-64 °C (lit.)
Boiling point:
100-102 °C/0.1 mmHg (lit.)
Density 
1.274 (estimate)
refractive index 
1.5500 (estimate)
Flash point:
100-102°C/0.1mm
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
pka
1.86±0.10(Predicted)
form 
Fine Crystalline Powder
color 
Beige to beige-brown
Water Solubility 
Slightly soluble in water.
BRN 
1365614
InChIKey
TWEQNZZOOFKOER-UHFFFAOYSA-N
CAS DataBase Reference
22288-78-4(CAS DataBase Reference)
EPA Substance Registry System
2-Thiophenecarboxylic acid, 3-amino-, methyl ester (22288-78-4)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39-36/37/39-22
WGK Germany 
3
RTECS 
XM8347500
TSCA 
Yes
HazardClass 
IRRITANT
HS Code 
29349990

MSDS

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Methyl 3-amino-2-thiophenecarboxylate Usage And Synthesis

Chemical Properties

white to light yellow crystal powder

Uses

Methyl 3-amino-2-thiophenecarboxylate was used in:

  • the synthesis of 4-nitro and 4-aminothienyl ureas
  • total synthesis of quinazolinocarboline alkaloids
  • preparation of thienopyrimidinone analogs

General Description

Methyl 3-amino-2-thiophenecarboxylate reacts with hydrazonoyl chlorides in the presence of triethylamine to yield corresponding N-arylamidrazones.

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