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52034-92-1

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52034-92-1 Usage

Chemical Properties

Solid

Uses

Different sources of media describe the Uses of 52034-92-1 differently. You can refer to the following data:
1. It is used as pharmaceutical intermediate. Benzoylthiophenes are allosteric enhancers (AE) of agonist activity at the A1 adenosine receptor.
2. Dicyclohexylacetic acid was used in the synthesis of 2,2-dicyclohexyl-1-(4′-methyl)-phenylethanone. It was also used in the synthesis of catena-poly [[trimethyltin (IV)]--2, 2-dicyclohexylacetato-2O: O′].

Check Digit Verification of cas no

The CAS Registry Mumber 52034-92-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,0,3 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 52034-92:
(7*5)+(6*2)+(5*0)+(4*3)+(3*4)+(2*9)+(1*2)=91
91 % 10 = 1
So 52034-92-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H24O2/c15-14(16)13(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h11-13H,1-10H2,(H,15,16)

52034-92-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H33523)  Dicyclohexylacetic acid, 98+%   

  • 52034-92-1

  • 5g

  • 1139.0CNY

  • Detail
  • Alfa Aesar

  • (H33523)  Dicyclohexylacetic acid, 98+%   

  • 52034-92-1

  • 25g

  • 5695.0CNY

  • Detail

52034-92-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-dicyclohexylacetic acid

1.2 Other means of identification

Product number -
Other names Dicyclohexyl-essigsaeure

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:52034-92-1 SDS

52034-92-1Relevant articles and documents

HETEROCUMULENES IN ACYLATION REACTIONS II. REACTIVITY OF ALKYL-SUBSTITUTED KETENES IN SPONTANEOUS HYDROLYSIS REACTIONS

Lyashchuk, S. N.,Skrypnik, Yu. G.

, p. 10 - 17 (2007/10/02)

The structures and electronic states of six ketenes were investigated by the semiempirical MNDO, MINDO/3, and AM1 quantum-chemical methods.The kinetics of the spontaneous hydrolysis of mono- and dialkylsubstituted ketenes in water and water-acetonitrile mixtures at 20 deg C were studied.The induction and steric effects of the substituents on the process rate were evaluated quantitatively in terms of a ρ? analysis.An increase in the number, length, and branching of the hydrocarbon substituents at the terminal carbon atom of the ketenes leads to a large decrease in the hydrolysis rate.The results of the calculations were compared with experimental data.Possible alternatives for the mechanism of the process are discussed.

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