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122-51-0

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122-51-0 Usage

Chemical Description

Triethyl orthoformate is used as a reactant in the synthesis of N,N′-diphenylimidazolinium Tetrafluoroborate.

Check Digit Verification of cas no

The CAS Registry Mumber 122-51-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,2 and 2 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 122-51:
(5*1)+(4*2)+(3*2)+(2*5)+(1*1)=30
30 % 10 = 0
So 122-51-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H16O3/c1-4-8-7(9-5-2)10-6-3/h7H,4-6H2,1-3H3

122-51-0 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (O0066)  Triethyl Orthoformate  >98.0%(GC)

  • 122-51-0

  • 25mL

  • 98.00CNY

  • Detail
  • TCI America

  • (O0066)  Triethyl Orthoformate  >98.0%(GC)

  • 122-51-0

  • 500mL

  • 236.00CNY

  • Detail
  • Alfa Aesar

  • (A13587)  Triethyl orthoformate, 98%   

  • 122-51-0

  • 100ml

  • 193.0CNY

  • Detail
  • Alfa Aesar

  • (A13587)  Triethyl orthoformate, 98%   

  • 122-51-0

  • 500ml

  • 350.0CNY

  • Detail
  • Alfa Aesar

  • (A13587)  Triethyl orthoformate, 98%   

  • 122-51-0

  • 2500ml

  • 1268.0CNY

  • Detail
  • Alfa Aesar

  • (A13587)  Triethyl orthoformate, 98%   

  • 122-51-0

  • 10000ml

  • 4332.0CNY

  • Detail
  • Sigma-Aldrich

  • (43103)  Triethylorthoformate  analytical standard

  • 122-51-0

  • 43103-1ML

  • 458.64CNY

  • Detail
  • Sigma-Aldrich

  • (43103)  Triethylorthoformate  analytical standard

  • 122-51-0

  • 43103-5ML

  • 1,817.01CNY

  • Detail
  • Sigma-Aldrich

  • (304050)  Triethylorthoformate  anhydrous, 98%

  • 122-51-0

  • 304050-100ML

  • 1,202.76CNY

  • Detail
  • Sigma-Aldrich

  • (304050)  Triethylorthoformate  anhydrous, 98%

  • 122-51-0

  • 304050-1L

  • 2,399.67CNY

  • Detail
  • Sigma-Aldrich

  • (T60453)  Triethylorthoformate  reagent grade, 98%

  • 122-51-0

  • T60453-500ML

  • 666.90CNY

  • Detail
  • Sigma-Aldrich

  • (T60453)  Triethylorthoformate  reagent grade, 98%

  • 122-51-0

  • T60453-1L

  • 1,000.35CNY

  • Detail

122-51-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Triethyl orthoformate

1.2 Other means of identification

Product number -
Other names Ethane, 1,1‘,1‘‘-[methylidynetris(oxy)]tris-

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:122-51-0 SDS

122-51-0Related news

Synthesis and reactivity of subvalent compounds. Part 13: Reaction of Triethyl orthoformate (cas 122-51-0) with amines and selenium—a convenient one-step three-component synthesis for selenoureas☆09/10/2019

Selenoureas are obtained by a novel three-component condensation reaction from metallic selenium, triethyl orthoformate and a primary or secondary amine. The reaction is carried out as solvent-free one pot-procedure at 180–190°C under inert gas with a reaction time of 8 h. The reaction was tes...detailed

Triethyl orthoformate (cas 122-51-0) as a new film-forming electrolytes solvent for lithium-ion batteries with graphite anodes09/09/2019

Triethyl orthoformate (TEOF) as a new solvent used in propylene carbonate (PC)-based electrolytes together with graphitic anodes in lithium-ion batteries has been investigated. It can be observed that TEOF was capable of suppressing the co-intercalation of PC solvated lithium-ions into the graph...detailed

Isobaric vapor–liquid equilibrium of systems containing Triethyl orthoformate (cas 122-51-0) at 101.3 kPa09/08/2019

Isobaric vapor–liquid equilibrium data of ethanol(1)-triethyl orthoformate(2), benzene(1)-triethyl orthoformate(2) and ethanol(1)-benzene(2)-triethyl orthoformate(3) were measured at 101.3 kPa and under a wide range of temperatures (349–420 K), using the Rose–Williams still modified by the au...detailed

Triethyl orthoformate (cas 122-51-0) mediated a novel crosslinking method for the preparation of hydrogels for tissue engineering applications: characterization and in vitro cytocompatibility analysis09/07/2019

This paper describes the development of a new crosslinking method for the synthesis of novel hydrogel films from chitosan and PVA for potential use in various biomedical applications. These hydrogel membranes were synthesized by blending different ratios of chitosan (CS) and poly(vinyl alcohol) ...detailed

122-51-0Relevant articles and documents

-

Tamborski,Post

, p. 1397 (1952)

-

-

Erickson

, p. 1569,1571 (1955)

-

Synthesis method of crude carboxylic ester (by machine translation)

-

Paragraph 0021; 0022, (2020/08/09)

The method is characterized in that the carboxylic ester and the ether are prepared by reacting a carboxylic ester with an ether at a certain temperature under the catalysis of a catalyst at a certain pressure for a certain time. (by machine translation)

Method for producing high purity orthoformate simple and convenient method of

-

Paragraph 0022-0028, (2017/12/04)

The invention provides a simple and convenient method for producing high-purity ortho-formate by using acrylonitrile byproduct hydrocyanic acid. The method comprises the following steps: firstly producing amine salt from the acrylonitrile byproduct hydrocyanic acid, fatty alcohol and hydrogen chloride, subsequently performing alcoholysis reaction on the presence of corresponding fatty alcohol so as to obtain an ortho-formate reaction liquid, adding a proper amount of an alkali substance in the generated ortho-formate reaction liquid, decomposing nitrogenous impurity compounds such as byproduct 1,3,5-s-triazine at certain temperature, wherein the decomposed product is nitrogen and solid formate with low boiling point, performing aftertreatment on the reaction liquid so as to obtain the high-purity ortho-formate through normal distillation. Therefore, the purpose of producing the high-purity ortho-formate with high yield is achieved.

Orthoester exchange: A tripodal tool for dynamic covalent and systems chemistry

Brachvogel, Ren-Chris,Von Delius, Max

, p. 1399 - 1403 (2015/02/05)

Reversible covalent reactions have become an important tool in supramolecular chemistry and materials science. Here we introduce the acid-catalyzed exchange of O,O,O-orthoesters to the toolbox of dynamic covalent chemistry. We demonstrate that orthoesters readily exchange with a wide range of alcohols under mild conditions and we disclose the first report of an orthoester metathesis reaction. We also show that dynamic orthoester systems give rise to pronounced metal template effects, which can best be understood by agonistic relationships in a three-dimensional network analysis. Due to the tripodal architecture of orthoesters, the exchange process described herein could find unique applications in dynamic polymers, porous materials and host-guest architectures.

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