Ethyl 4-oxocyclohexanecarboxylate

What is Ethyl 4-oxocyclohexanecarboxylate , cas no. 17159-79-4,a producer telling you the result.

                                                        CAS NO. 17159-79-4

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To begin with, let us tell you what is the basic information of  Ethyl 4-oxocyclohexanecarboxylate Cas No. 17159-79-4 ?

 

MDL No.

MFCD00013285

Molecular Weight

170.21

Density

1.1±0.1 g/cm3

Boiling Point

248.8±33.0 °C at 760 mmHg

Molecular Formula

C9H14O3

Flash Point

103.8±25.4 °C

 

Like many stuff, it has many synonyms as follows

ethyl 4-oxocyclohexane-1-carboxylate

4-(Ethoxycarbonyl)cyclohexanone,Ethyl cyclohexanone-4-carboxylate

4-Oxocyclohexanecarboxylic acid ethyl ester

Ethyl 4-Cyclohexanonecarboxylate

L6VTJ DVO2

4-(Ethoxycarbonyl)cyclohexan-1-one

Cyclohexanecarboxylic acid, 4-oxo-, ethyl ester

Ethyl cyclohexanone-4-carboxylate

Ethyl 4-Oxo-Cyclohexanecarboxylate

Ethyl 4-oxocyclohexanecarboxylate

4-(Ethoxycarbonyl)cyclohexanone

 

The chemical is very special

 

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Molecular structure data

1. Molar refractive index: 43.38

2. Molar volume (m3/mol): 157.0

3. Isometric volume (90.2K): 389.5

4. Surface tension (3.0 dyne/cm): 37.8

5. Polarization rate (0.5 10-24cm3): 17.19

Computational Chemistry Data

1. Reference value for hydrophobic parameter calculation (XlogP): 0.6

2. Number of hydrogen bond donors: 0

3. Number of hydrogen bond receptors: 3

4. Number of rotatable chemical bonds: 3

5. Number of tautomers: 2

6. Topological molecule polarity surface area 43.4

7. Number of heavy atoms: 12

8. Surface charge: 0

9. Complexity: 176

10. Number of Isotope Atoms: 0

11. Determine the number of atomic structure centers: 0

12. Number of uncertain atomic structure centers: 0

13. Determine the number of chemical bond stereocenters: 0

14. Number of uncertain chemical bond stereocenters: 0

15. Number of covalent bond units: 1

Second, the Synthetic Route we will recommend is the most important for your reference?

 

First, synthesis line of Ethyl 4-oxocyclohexanecarboxylate Cas No. 17159-79-4 as follows

 

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1. Synthesis of p-cyclohexanone ethyl formate by trans-4-hydroxycyclohexane ethyl formate in a yield of approximately 97%;

 

2. Ethyl p-cyclohexanone formate was synthesized by using tetrapropylamine perrutheniate (TPAP), trans-4-hydroxycyclohexane formate, and N-methylmorpholine nitrogen oxide, with a yield of approximately 95%;

 

 

Third, what is the usage of Ethyl 4-oxocyclohexanecarboxylate Cas No. 17159-79-4  pleas see below

 

Main Usage:

Ethyl formate of cyclohexanone is a derivative of cyclohexanone, used as an organic synthesis intermediate and pharmaceutical intermediate in laboratory research and development processes and chemical and pharmaceutical synthesis processes. Ethyl formate of cyclohexanone is a derivative of cyclohexanone, used for studying the catalytic properties of cyclohexanone monooxygenases and their mutants

 

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Other usages as below

 

One kind of raw material for producing 4,4-bis[4-(quinolin-2-ylmethoxy)phenyl]cyclohexane-1-carboxylic acid  cas no 195050-52-3 ,which is as follows

 

One kind of raw material for producing  2-(1,4-dioxaspiro[4.5]decan-8-ylidene)ethoxymethoxy-trimethylsilan  cas no 182227-16-3 which is as follows

 

Besides Safety Information of Ethyl 4-oxocyclohexanecarboxylate Cas No. 17159-79-4 is also important when handling it

Hazard Codes

Xi

H.S. Code

2918300090

 

What is the appearance of  Ethyl 4-oxocyclohexanecarboxylate Cas No. 17159-79-4?   Please see the picture of Ethyl 4-oxocyclohexanecarboxylate Cas No. 17159-79-4, below

 

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Specification of Ethyl 4-oxocyclohexanecarboxylate Cas No. 17159-79-4, is below

Appearance: Clear colorless to yellow liquid

Assay :≥99.00% by GC

Density: 1.068

Water Solubility: Insoluble

IR identity: conform

.HNMR  picture of  Ethyl 4-oxocyclohexanecarboxylate Cas No. 17159-79-4 is as follows,

 

IR  picture of  Ethyl 4-oxocyclohexanecarboxylate Cas No. 17159-79-4  is as follows,

 

Reference of  Article cited for your reference below,

(1)

TEMPO-Mediated Convergent Synthesis of Benzoxazoles from Primary Amines and Cyclohexanones

Publication Name: Synfacts

Publication Date: 2022-09-20

DOI: 10.1055/s-0042-1752975

(2)

New endoperoxides highly active in vivo and in vitro against artemisinin-resistant Plasmodium falciparum

Publication Name: Malaria Journal

Publication Date: 2018-04-03

PMID: 29615130

DOI: 10.1186/s12936-018-2281-x

(3)

Synthesis of a GPR40 Superagonist

Publication Name: Synfacts

Publication Date: 2019-02-15

DOI: 10.1055/s-0037-1611187