Basic information Safety Supplier Related

5-(DIMETHYLAMINO)THIOPHENE-2-CARBALDEHYDE

Basic information Safety Supplier Related

5-(DIMETHYLAMINO)THIOPHENE-2-CARBALDEHYDE Basic information

Product Name:
5-(DIMETHYLAMINO)THIOPHENE-2-CARBALDEHYDE
Synonyms:
  • 5-dimethylamino-2-thiophenecarboxaldehyde
  • 5-(dimethylamino)thiophene-2-carbaldehyde(SALTDATA: FREE)
  • 2-Thiophenecarboxaldehyde, 5-(dimethylamino)-
CAS:
24372-46-1
MF:
C7H9NOS
MW:
155.22
Mol File:
24372-46-1.mol
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5-(DIMETHYLAMINO)THIOPHENE-2-CARBALDEHYDE Chemical Properties

Boiling point:
280.3±25.0 °C(Predicted)
Density 
1?+-.0.06 g/cm3(Predicted)
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
Chloroform (Slightly), Methanol (Slightly)
pka
1.42±0.30(Predicted)
form 
Solid
color 
Dark Red to Very Dark Brown
InChI
InChI=1S/C7H9NOS/c1-8(2)7-4-3-6(5-9)10-7/h3-5H,1-2H3
InChIKey
RRQFJMCAGDOEPI-UHFFFAOYSA-N
SMILES
C1(C=O)SC(N(C)C)=CC=1
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Safety Information

Safety Statements 
24/25
HazardClass 
IRRITANT
HS Code 
29349990
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5-(DIMETHYLAMINO)THIOPHENE-2-CARBALDEHYDE Usage And Synthesis

Chemical Properties

Light yellow solid

Synthesis

4701-17-1

124-40-3

24372-46-1

General procedure for the synthesis of 5-dimethylamino-2-thiophenecarboxaldehyde (30): 5-bromo-2-thiophenecarboxaldehyde (1 g, 5.23 mmol) was mixed with dimethylamine (1.64 mL, 15.69 mmol) in pure water (3 mL). The reaction mixture was stirred at 100 °C for 12 hours. After completion of the reaction, it was extracted with chloroform (50 mL x 2), the organic phases were combined and washed with purified water (50 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by medium pressure preparative chromatography with ethyl acetate/hexane (1/1, v/v) as eluent to afford the target compound 30 (670 mg, 82.5% yield).1H NMR (300 MHz, CDCl3) δ 3.10 (s, 6H), 5.96 (s, 1H), 7.45 (s, 1H), 9.44 (s, 1H).

References

[1] Synlett, 1998, # 4, p. 383 - 384
[2] Patent: EP2030635, 2009, A1. Location in patent: Page/Page column 26; 50
[3] Chemical Communications, 2015, vol. 51, # 96, p. 17124 - 17127
[4] Patent: CN107090190, 2017, A. Location in patent: Paragraph 0046; 0047; 0048; 0049
[5] Journal of the American Chemical Society, 2001, vol. 123, # 12, p. 2810 - 2824

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