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17159-80-7

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  • High quality Ethyl 4- Hydroxycyclohexanecarboxylate(Mixture Of Cis & Trans Isomers) supplier in China

    Cas No: 17159-80-7

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17159-80-7 Usage

Description

ETHYL 4-HYDROXYCYCLOHEXANECARBOXYLATE, also known as Ethyl 4-hydroxycyclohexanecarboxylate (cis + trans), is an organic compound that serves as a crucial intermediate in the synthesis of various chemicals and pharmaceuticals. Its unique chemical structure allows it to be a versatile building block in the creation of different compounds.

Uses

Used in Chemical Synthesis:
ETHYL 4-HYDROXYCYCLOHEXANECARBOXYLATE is used as a chemical intermediate for the synthesis of other chemicals. It plays a vital role in the production of various compounds due to its reactive functional groups and compatibility with a wide range of chemical reactions.
Used in Pharmaceutical Industry:
ETHYL 4-HYDROXYCYCLOHEXANECARBOXYLATE is used as a pharmaceutical intermediate for the development of new drugs and medications. Its unique structure and reactivity make it an essential component in the synthesis of various pharmaceutical compounds, contributing to the advancement of medical treatments and therapies.

Synthesis Reference(s)

The Journal of Organic Chemistry, 30, p. 4145, 1965 DOI: 10.1021/jo01023a039

Check Digit Verification of cas no

The CAS Registry Mumber 17159-80-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,5 and 9 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17159-80:
(7*1)+(6*7)+(5*1)+(4*5)+(3*9)+(2*8)+(1*0)=117
117 % 10 = 7
So 17159-80-7 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O3/c1-2-12-9(11)7-3-5-8(10)6-4-7/h7-8,10H,2-6H2,1H3

17159-80-7 Well-known Company Product Price

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  • Alfa Aesar

  • (B25572)  Ethyl 4-hydroxycyclohexanecarboxylate, cis + trans, 97%   

  • 17159-80-7

  • 5g

  • 607.0CNY

  • Detail
  • Alfa Aesar

  • (B25572)  Ethyl 4-hydroxycyclohexanecarboxylate, cis + trans, 97%   

  • 17159-80-7

  • 25g

  • 1870.0CNY

  • Detail

17159-80-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 4-Hydroxycyclohexanecarboxylate

1.2 Other means of identification

Product number -
Other names Ethyl 4-hydroxycyclohexanecarboxylate

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:17159-80-7 SDS

17159-80-7Relevant articles and documents

Kwart,Takeshita

, p. 2833 (1962)

HETEROARYLDIHYDROPYRIMIDINE DERIVATIVES AND METHODS OF TREATING HEPATITIS B INFECTIONS

-

Page/Page column 106, (2019/01/17)

Provided herein are compounds useful for the treatment of HBV infection in a subject in need thereof, pharmaceutical compositions thereof, and methods of inhibiting, suppressing, or preventing HBV infection in the subject.

A biocatalytic/reductive etherification approach to substituted piperidinyl ethers

Kuethe, Jeffrey T.,Janey, Jacob M.,Truppo, Matthew,Arredondo, Juan,Li, Tao,Yong, Kelvin,He, Shuwen

, p. 4563 - 4570 (2014/06/10)

A synthetically useful protocol has been developed for the preparation of highly functionalized piperidinyl ethers. Biocatalytic reduction of cyclhexanones 7, 10, and 14 allows for the preparation of both cis- and trans diastereomers with an extremely high degree of stereochemical control. Reductive etherification of the corresponding trimethylsilylethers with 1-(benzyloxycarbonyl)-4-piperidinone 17 in the presence of triethylsilane and catalytic TMSO-Tf provides the desired piperidinyl ethers in good to excellent yields. Finally hygrogenolysis of the nitrogen protecting group leads to piperidinyl ethers in near quantitative yields. Application of the methodology to a range of piperidinyl ethers, including the core scaffolds of diphenylpyraline and ebastine, is also described.

IMIDAZOLE DERIVATIVES

-

Page/Page column 60, (2013/02/27)

Described herein are compounds of formula (I), The compounds of formula I act as DGAT1 inhibitors and can be useful in preventing, treating or acting as a remedial agent for hyperlipidemia, diabetes mellitus and obesity.

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