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41233-93-6

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41233-93-6 Usage

Description

POTASSIUM 2-METHYL-2-BUTOXIDE, also known as potassium tert-pentyloxide, is a versatile compound with a wide range of applications across various industries. It is characterized by its reactivity and ability to act as a catalyst in numerous chemical processes.
Used in Organic Synthesis:
POTASSIUM 2-METHYL-2-BUTOXIDE is used as a reagent for various organic synthesis processes due to its ability to facilitate chemical reactions and improve overall yields.
Used in Agrochemicals:
In the Agrochemical Industry, POTASSIUM 2-METHYL-2-BUTOXIDE is used as a catalyst for the synthesis of various agrochemical products, enhancing the efficiency and effectiveness of these compounds.
Used in Pharmaceuticals:
POTASSIUM 2-METHYL-2-BUTOXIDE is used as a catalyst in the pharmaceutical industry to facilitate the synthesis of various drugs, contributing to the development of new and improved medications.
Used in Colorants and Aroma Chemicals:
In the production of colorants and aroma chemicals, POTASSIUM 2-METHYL-2-BUTOXIDE is used as a catalyst to improve the synthesis of these compounds, leading to better quality and more vibrant products.
Used in Detergent Manufacturing:
POTASSIUM 2-METHYL-2-BUTOXIDE is used as a catalyst in the manufacturing of detergents, helping to create more effective cleaning agents.
Used in Biodiesel Production:
In the Biodiesel Industry, POTASSIUM 2-METHYL-2-BUTOXIDE is used as a catalyst to improve the production process and enhance the quality of the final product.
Used in Polymerization:
POTASSIUM 2-METHYL-2-BUTOXIDE is used as a catalyst in polymerization processes, contributing to the development of new and improved polymer materials.
Used in Isomerization:
POTASSIUM 2-METHYL-2-BUTOXIDE is used as a catalyst in isomerization reactions, such as the synthesis of [RuClPh(CO)(H2IMes)(PCy3)] from second-generation Grubbs metathesis catalyst, [RuCl2(=CHPh)(H2IMes)(PCy3)], and benzyl alcohol. This complex is a solid, air-stable, and highly active isomerization catalyst, showcasing the versatility of POTASSIUM 2-METHYL-2-BUTOXIDE in various chemical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 41233-93-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,2,3 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 41233-93:
(7*4)+(6*1)+(5*2)+(4*3)+(3*3)+(2*9)+(1*3)=86
86 % 10 = 6
So 41233-93-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H11O.K/c1-4-5(2,3)6;/h4H2,1-3H3;/q-1;+1

41233-93-6 Well-known Company Product Price

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  • Alfa Aesar

  • (41394)  Potassium tert-pentyloxide, 14-18% w/v in cyclohexane   

  • 41233-93-6

  • 5g

  • 284.0CNY

  • Detail
  • Alfa Aesar

  • (41394)  Potassium tert-pentyloxide, 14-18% w/v in cyclohexane   

  • 41233-93-6

  • 25g

  • 1014.0CNY

  • Detail
  • Alfa Aesar

  • (41394)  Potassium tert-pentyloxide, 14-18% w/v in cyclohexane   

  • 41233-93-6

  • 100g

  • 3381.0CNY

  • Detail
  • Alfa Aesar

  • (L15111)  Potassium tert-pentyloxide, 25% w/w in toluene   

  • 41233-93-6

  • 250ml

  • 712.0CNY

  • Detail
  • Alfa Aesar

  • (L15111)  Potassium tert-pentyloxide, 25% w/w in toluene   

  • 41233-93-6

  • 1000ml

  • 2228.0CNY

  • Detail
  • Aldrich

  • (702757)  Potassiumtert-pentoxidesolution  2 M in THF

  • 41233-93-6

  • 702757-100ML

  • 2,515.50CNY

  • Detail
  • Aldrich

  • (702757)  Potassiumtert-pentoxidesolution  2 M in THF

  • 41233-93-6

  • 702757-500ML

  • 12,296.70CNY

  • Detail

41233-93-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name Potassium 2-Methyl-2-Butoxide

1.2 Other means of identification

Product number -
Other names POTASSIUM 2-METHYL-2-BUTOXIDE

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:41233-93-6 SDS

41233-93-6Relevant articles and documents

6-Oxoestradiols from estradiols: Exploiting site selective metalation of aralkyl systems with superbases

Tedesco,Fiaschi,Napolitano

, p. 1493 - 1495 (1995)

3-O-Protected estradiol derivatives undergo metalation at C-6 when exposed to a fourfold excess of the reagent consisting of an equimolar mixture of lithium diisopropylamide and potassium 1,1-dimethylpropoxide (3 h, THF, -78°C). The metalated intermediates can be oxidized by quenching with trimethyl borate followed by treatment with hydrogen peroxide, thus allowing the introduction of a 6-hydroxy group into the estradiol framework. Further oxidation of the 6-hydroxy group gives O-protected 6-oxoestradiols.

Antiangiogenic agents

-

Page/Page column 15, (2008/06/13)

Compositions and methods for treating mammalian diseases or conditions characterized by undesirable angiogenesis by administering an effective amount of a compound of the formulae: wherein Ra is selected from —OCH3, —OCH2CH3 or —CCCH3; and Z is selected from >C(H)—OH, >C(H)—O-alkyl, >C(H)—O-sulfamate, where alkyl is a linear, branched and/or cyclic hydrocarbon chain comprising 1 to 10 carbons.

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