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5683-31-8

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5683-31-8 Usage

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.

Check Digit Verification of cas no

The CAS Registry Mumber 5683-31-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,8 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5683-31:
(6*5)+(5*6)+(4*8)+(3*3)+(2*3)+(1*1)=108
108 % 10 = 8
So 5683-31-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H10O2Si/c1-9(2,3)5-4-6(7)8/h1-3H3,(H,7,8)

5683-31-8 Well-known Company Product Price

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  • Alfa Aesar

  • (H53380)  3-(Trimethylsilyl)propiolic acid, 97%   

  • 5683-31-8

  • 1g

  • 772.0CNY

  • Detail
  • Alfa Aesar

  • (H53380)  3-(Trimethylsilyl)propiolic acid, 97%   

  • 5683-31-8

  • 5g

  • 2894.0CNY

  • Detail
  • Alfa Aesar

  • (H53380)  3-(Trimethylsilyl)propiolic acid, 97%   

  • 5683-31-8

  • 25g

  • 11576.0CNY

  • Detail

5683-31-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(Trimethylsilyl)propynoic acid

1.2 Other means of identification

Product number -
Other names 3-trimethylsilylprop-2-ynoic acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5683-31-8 SDS

5683-31-8Relevant articles and documents

Design and Remarkable Efficiency of the Robust Sandwich Cluster Composite Nanocatalysts ZIF-8@Au25@ZIF-67

Yun, Yapei,Sheng, Hongting,Bao, Kang,Xu, Li,Zhang, Yu,Astruc, Didier,Zhu, Manzhou

supporting information, p. 4126 - 4130 (2020/03/05)

Heterogeneous catalysts with precise surface and interface structures are of great interest to decipher the structure-property relationships and maintain remarkable stability while achieving high activity. Here, we report the design and fabrication of the new sandwich composites ZIF-8@Au25@ZIF-67[tkn] and ZIF-8@Au25@ZIF-8[tkn] [tkn = thickness of shell] by coordination-assisted self-assembly with well-defined structures and interfaces. The composites ZIF-8@Au25@ZIF-67 efficiently catalyzed both 4-nitrophenol reduction and terminal alkyne carboxylation with CO2 under ambient conditions with remarkably improved activity and stability, compared to the simple components Au25/ZIF-8 and Au25@ZIF-8, highlighting the highly useful function of the ultrathin shell. In addition, the performances of these composite sandwich catalysts are conveniently regulated by the shell thickness. This concept and achievements should open a new avenue to the targeted design of well-defined nanocatalysts with enhanced activities and stabilities for challenging reactions.

Carboxylation of terminal alkynes promoted by silver carbamate at ambient pressure

Bresciani, Giulio,Marchetti, Fabio,Pampaloni, Guido

, p. 10821 - 10825 (2019/07/15)

Transition metal carbamates constitute a class of compounds with unique properties, however their catalytic potential has been sparingly explored so far. The easily available silver N,N-dimethylcarbamate, Ag(O2CNMe2), worked as a catalyst in the carboxylation reaction of terminal alkynes with CO2 at atmospheric pressure. Different reaction parameters (solvent, base, temperature, time and the amount of catalyst) were investigated in order to establish the optimal conditions.

Method for preparing acid through oxidating alcohols or aldehydes by oxygen

-

Paragraph 0051; 0052; 0053; 0054; 0091; 0092; 0093, (2017/09/29)

The invention provides a method for preparing acid through oxidating alcohols or aldehydes by using oxygen or oxygen in air as an oxidant. The method comprises the steps: oxidating the alcohols or aldehydes to produce the acid at room temperature in an organic solvent in a manner of taking ferric nitrate (Fe(NO3)3.9H2O), 2,2,6,6-tetramethylpiperidyl nitrogen oxide (TEMPO) and an inorganic halide as catalysts and taking the oxygen or air as an oxidant, and oxidating diols to produce lactone; or, carrying out a reaction on the aldehydes, which serve as a raw material, under neutral conditions by taking ferric nitrate as a catalyst, and oxidating the aldehydes to produce the acid and peroxy acid. The method has the advantages that the method is environmentally friendly, the cost is low, the yield is high, the atomic economical efficiency is high, the compatibility of substrate functional groups is good, the reaction conditions are mild, a reaction scale can be enlarged, and the like, so that the method is suitable for being applied to industrial production.

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