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3-Methyl-2-thiophenecarboxaldehyde

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3-Methyl-2-thiophenecarboxaldehyde Basic information

Product Name:
3-Methyl-2-thiophenecarboxaldehyde
Synonyms:
  • 3-Methylthiophene-2-aldehyde 2-Formyl-3-methylthiophene
  • 2-FORMYL-3-METHYLTHIOPHENE
  • AKOS BBS-00003151
  • 2-Formyl-3-methylthiophene, 3-Methyl-2-thenaldehyde
  • 3-Methylthiophene-2-carboxaldehyde,tech.90%
  • 3-Methyl-2-thiophenecarboxaldehyde 90%, technical grade
  • 3-Methylthiophene-2-carbaldehyde for synthesis
  • 3-Methylthiophene-2-carboxaldehyde, 97.5%
CAS:
5834-16-2
MF:
C6H6OS
MW:
126.18
EINECS:
227-418-8
Product Categories:
  • Building Blocks
  • Heterocyclic Building Blocks
  • Thiophene&Benzothiophene
  • Heterocyclic Compounds
  • Thiophenes
Mol File:
5834-16-2.mol
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3-Methyl-2-thiophenecarboxaldehyde Chemical Properties

Melting point:
260-262 °C
Boiling point:
78-80 °C (15 mmHg)
Density 
1.17 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.587(lit.)
Flash point:
180 °F
storage temp. 
Store below +30°C.
form 
Liquid
Specific Gravity
1.170
color 
Clear yellow to brown
Water Solubility 
insoluble
Sensitive 
Air Sensitive
BRN 
107874
LogP
1.458 (est)
CAS DataBase Reference
5834-16-2(CAS DataBase Reference)
NIST Chemistry Reference
3-Methyl-2-thiophenecarboxaldehyde(5834-16-2)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
23-24/25-36/37/39-26-36-7/9-37
WGK Germany 
3
Hazard Note 
Irritant
HazardClass 
IRRITANT, AIR SENSITIVE
HS Code 
29349990

MSDS

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3-Methyl-2-thiophenecarboxaldehyde Usage And Synthesis

Chemical Properties

clear yellow to brown liquid

Uses

3-Methyl-2-thiophenecarboxaldehyde is used in the synthesis of 2,3-dimethyl-5-(2,6,10-trimethylundecyl)thiophene. It is also used to investigate versatile bioconversion capacity of baker′s yeast for the generation of thiols from cysteine-aldehyde conjugates.

Uses

3-Methyl-2-thiophenecarboxaldehyde was used in the synthesis of 2,3-dimethyl-5-(2,6,10-trimethylundecyl)thiophene. It was used to investigate versatile bioconversion capacity of baker′s yeast for the generation of thiols from cysteine-aldehyde conjugates.

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