ChemicalBook > CAS DataBase List > CHEMBRDG-BB 4004130

CHEMBRDG-BB 4004130

Product Name
CHEMBRDG-BB 4004130
CAS No.
30433-92-2
Chemical Name
CHEMBRDG-BB 4004130
Synonyms
AKOS ISYA01283;RARECHEM AN KA 0153;CHEMBRDG-BB 4004130;UKRORGSYN-BB BBV-182415;2-(5-METHYL-2-THIENYL)ETHANAMINE;2-Thiopheneethanamine, 5-methyl-;2-(5-methylthiophen-2-yl)ethanamine;2-(5-METHYL-THIOPHEN-2-YL)-ETHYLAMINE;2-(5-methyl-2-thienyl)ethanamine(SALTDATA: FREE)
CBNumber
CB7496059
Molecular Formula
C7H11NS
Formula Weight
141.23
MOL File
30433-92-2.mol
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CHEMBRDG-BB 4004130 Property

storage temp. 
2-8°C(protect from light)
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Safety

HazardClass 
IRRITANT
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

TRC
Product number
M222843
Product name
2-(5-Methyl-2-thienyl)ethanamine
Packaging
10mg
Price
$45
Updated
2021/12/16
TRC
Product number
M222843
Product name
2-(5-Methyl-2-thienyl)ethanamine
Packaging
50mg
Price
$90
Updated
2021/12/16
Matrix Scientific
Product number
033432
Product name
2-(5-Methyl-thiophen-2-yl)-ethylamine
Packaging
500mg
Price
$200
Updated
2021/12/16
AK Scientific
Product number
9610AD
Product name
2-(5-Methyl-thiophen-2-yl)-ethylamine
Packaging
500mg
Price
$320
Updated
2021/12/16
Apolloscientific
Product number
OR322779
Product name
2-(5-Methyl-2-thienyl)ethanamine
Packaging
500mg
Price
$356
Updated
2021/12/16
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CHEMBRDG-BB 4004130 Chemical Properties,Usage,Production

Synthesis

117693-20-6

30433-92-2

b) Step 2: Synthesis of 2-(5-methyl-2-thienyl)ethylamine A solution of 6.9 g (175 mmol) of 2-methyl-5-((E)-2-nitrovinyl)-thiophene dissolved in 150 mL of diethyl ether was slowly added dropwise to a suspension of 6.9 g (40.78 mmol) of LiAlH4 in 70 mL of ethyl ether under nitrogen protection, controlling the temperature to 20 to 25 °C. After dropwise addition, the reaction mixture was heated to reflux for 5 hours. After completion of the reaction, the mixture was cooled to 0 °C and the reaction was quenched by sequentially adding 28 mL of water and 7 mL of 5N NaOH solution. The white solid was removed by filtration and the filter cake was washed with ethyl acetate. The filtrates were combined and concentrated under reduced pressure to remove the solvent. The residue was purified by distillation under reduced pressure to give 4.98 g (86% yield) of the target compound 2-(5-methyl-2-thienyl)ethylamine as a colorless liquid.MS (m/e): 142.2 (MH+).

References

[1] Patent: US2008/249125, 2008, A1. Location in patent: Page/Page column 11-12
[2] Journal of Organic Chemistry, 1950, vol. 15, p. 807,810

CHEMBRDG-BB 4004130 Preparation Products And Raw materials

Raw materials

Preparation Products

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