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3-(TRIMETHYLSILYL)PROPIOLIC ACID

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3-(TRIMETHYLSILYL)PROPIOLIC ACID Basic information

Product Name:
3-(TRIMETHYLSILYL)PROPIOLIC ACID
Synonyms:
  • 3-(TRIMETHYLSILYL)PROPIOLIC ACID
  • 3-(TRIMETHYLSILYL)PROPYNOIC ACID
  • TIMTEC-BB SBB009048
  • 3-(Trimethylsilyl)propynoic acid,3-(Trimethylsilyl)propiolic acid
  • 3-(TRIMETHYLSILYL)PROPIOLIC ACID 95%
  • 3-(Trimethylsilyl)propynoic acid 98%
  • 3-(Trimethylsi
  • 3-trimethylsilyl-2-propynoic acid
CAS:
5683-31-8
MF:
C6H10O2Si
MW:
142.23
Product Categories:
  • Building Blocks
  • Carbonyl Compounds
  • Carboxylic Acids
  • Chemical Synthesis
  • Organic Building Blocks
  • C6
Mol File:
5683-31-8.mol
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3-(TRIMETHYLSILYL)PROPIOLIC ACID Chemical Properties

Melting point:
47-49 °C (lit.)
Boiling point:
105-110 °C/10 mmHg (lit.)
Density 
1.006±0.06 g/cm3(Predicted)
Flash point:
205 °F
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
solubility 
Soluble in methanol.
form 
solid
pka
1.88±0.10(Predicted)
color 
White to Almost white
Hydrolytic Sensitivity
4: no reaction with water under neutral conditions
BRN 
1755674
InChI
InChI=1S/C6H10O2Si/c1-9(2,3)5-4-6(7)8/h1-3H3,(H,7,8)
InChIKey
IPEATTYBFBRNEB-UHFFFAOYSA-N
SMILES
C(O)(=O)C#C[Si](C)(C)C
CAS DataBase Reference
5683-31-8(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
1-10
TSCA 
No
HS Code 
29319090

MSDS

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3-(TRIMETHYLSILYL)PROPIOLIC ACID Usage And Synthesis

Uses

3-(Trimethylsilyl)propiolic acid may be used in the regioselective preparation of 1,5-trisubstituted 1H-1,2,3-triazoles. It is also used as pharmaceutical intermediate.

Synthesis

2975-46-4

5683-31-8

The general procedure for the synthesis of 3-(trimethylsilyl)propynoic acid from 3-trimethylsilylpropynal was as follows: in a reaction test tube, trans-2-decene (167 mg, 1.0 mmol) was added to a mixture containing Fe(NO3)3-9H2O (4.1 mg, 0.010 mmol) and CF3COONa (28 mg, 0.20 mmol) in an EtOAc (0.50 mL) in suspension. An O2 balloon (1 atm) was attached to the top of the test tube to displace the internal atmosphere with O2. After the reaction mixture was stirred at 25 °C for 16 h, EtOAc (3 mL) and 1 M HCl aqueous solution (1 mL) were added and the resulting two-phase mixture was stirred for 1 min. The organic phase was separated and the aqueous phase was extracted with EtOAc (3 mL × 2). After combining the organic phases, quantitative biphenyl (as an internal standard for NMR analysis) was added. The conversion of the substrate and the yield of the product were determined by NMR analysis (400 MHz, CDCl3, 25 °C). Products were identified by comparing the NMR signals of real samples. Each reaction was repeated twice to ensure reproducible results.

References

[1] Chemistry Letters, 2016, vol. 45, # 2, p. 188 - 190

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