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2-Piperidinecarboxylic acid, 5-hydroxy-, methyl ester, (2S,5S)(9CI), also known as (2S,5S)-5-Hydroxypiperidine-2-carboxylic acid methyl ester, is a chemical compound belonging to the class of piperidinecarboxylic acids. It has a molecular formula of C7H13NO3 and a molecular weight of 159.18 g/mol. This derivative of 5-hydroxypiperidinecarboxylic acid is recognized for its therapeutic potential and is extensively studied for its potential applications in the treatment of various diseases and medical conditions. It plays a significant role in pharmaceutical research and development due to its promising applications.
Used in Pharmaceutical Industry:
2-Piperidinecarboxylic acid, 5-hydroxy-, methyl ester, (2S,5S)(9CI) is used as a key intermediate in the synthesis of various drugs and medicinal compounds. Its unique chemical structure and properties make it a valuable component in the development of new pharmaceuticals.
Used in Drug Development:
2-Piperidinecarboxylic acid, 5-hydroxy-, methyl ester, (2S,5S)(9CI) is used as a precursor in the development of new drugs for the treatment of various diseases and medical conditions. Its therapeutic potential is currently being explored in research studies.
Used in Research and Development:
2-Piperidinecarboxylic acid, 5-hydroxy-, methyl ester, (2S,5S)(9CI) is used as a research compound to study its potential uses in the treatment of various diseases and medical conditions. Its unique properties and therapeutic potential make it an important compound in pharmaceutical research and development.

695183-75-6

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695183-75-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 695183-75-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,9,5,1,8 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 695183-75:
(8*6)+(7*9)+(6*5)+(5*1)+(4*8)+(3*3)+(2*7)+(1*5)=206
206 % 10 = 6
So 695183-75-6 is a valid CAS Registry Number.

695183-75-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name cis-5(S)-hydroxy-2(S)-pipecolic acid methyl ester

1.2 Other means of identification

Product number -
Other names 5-(S)-hydroxy-2-(S)-pipecolic acid methyl ester

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:695183-75-6 SDS

695183-75-6Relevant academic research and scientific papers

Five-membered heteroaromatic derivative, preparation method and application thereof

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Paragraph 1146-1150, (2021/07/08)

The invention belongs to the technical field of medicines, and particularly relates to a five-membered heteroaromatic compound, a composition, a preparation method and application thereof. The compound or the composition can be used as an inhibitor of a retinoid-related orphan receptor [gamma]t (ROR [gamma]t). The invention also relates to a method for preparing the compound and the composition, and application of the compound and the composition in treatment or prevention of ROR [gamma]t-mediated cancers, inflammations or autoimmune diseases of mammals, especially human beings.

ROR [gamma]t inhibitor, preparation method and application thereof

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Paragraph 0993; 0996-0998, (2021/07/08)

The invention relates to the technical field of medicines, in particular to an ROR [gamma]t inhibitor, a preparation method and application thereof. The invention also relates to a pharmaceutical composition containing the compound, a method for preparing the pharmaceutical composition, and application of the compound or the pharmaceutical composition in treatment or prevention of ROR [gamma]t-mediated cancers, inflammations or autoimmune diseases of mammals, especially human beings.

RORγ ANTAGONIST AND APPLICATION THEREOF IN MEDICINE

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Paragraph 00733; 00745; 00757; 00770, (2020/02/06)

Provided herein are compounds as RORγ antagonist having Formula (I). The compounds or pharmaceutical composition thereof can be used for regulating Retinoid-related orphan receptor gamma t (RORγt). Also provided herein are methods of preparation of the compounds and composition thereof, and uses thereof in treating or preventing RORγt mediated inflammation or autoimmune diseases in mammals, particularly humans.

CRYSTAL OF DIAZABICYCLEOCTANE DERIVATE AND METHOD FOR PRODUCING THE SAME

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Paragraph 0118, (2017/02/02)

The present invention provides a crystal of diazabicycleoctane derivate represented by the following formula (VII), especially formula (VII-1), and a method for producing the same.

Production method for diazabicyclooctane derivative and intermediary body thereof

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Paragraph 0281; 0282; 0283, (2016/10/08)

The present invention provides a production method for a diazabicyclooctane derivative expressed by formula (IV), and an intermediary body thereof (in the formula: P is an acid-removable NH protective group; R1 represents a 2, 5-dioxopyrrolidine-1-yl, a 1, 3-dioxo-3a, a 4, 7, 7a-tetrahydro-1H-isoindole-2(3H)-yl, a 1, 3-dioxohexahydro-1H-isoindole-2(3H)-yl, or a 3, 5-dioxo-4-azatricyclo[5.2.1.02, 6]deca-8-en-4-yl; R2 represents hydrogen, C1CO-, or C13COCO-, R3 represents a C1-6 alkyl or a heterocyclyl, or joins with a bonded -O-NH- to form a 3-7 member heterocyclyl ring; and OBn represents a benzyloxy).

CRYSTALLINE FORMS OF DIAZABICYCLOOCTANE DERIVATIVE AND PRODUCTION PROCESS THEREOF

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Paragraph 0192, (2016/10/11)

A crystalline form of a diazabicyclooctane derivative represented by the following Formula (VII), and processes for producing the same:

(2S,5R/2R,5S)-Aminoethylpipecolyl aepip-aegPNA chimera: Synthesis and duplex/triplex stability

Shirude, Pravin S.,Kumar, Vaijayanti A.,Ganesh, Krishna N.

, p. 9485 - 9491 (2007/10/03)

This article reports the design and facile synthesis of novel chiral six-membered PNA analogues (2S,5R/2R,5S)-1-(N-Boc-aminoethyl)-5-(thymin-1-yl) pipecolic acid, aepipPNA IV that upon incorporation into standard aegPNA sequences effected stabilization of

Chimeric peptide nucleic acids incorporating (2S,5R)-aminoethyl pipecolyl units: Synthesis and DNA binding studies

Shirude, Pravin S.,Kumar, Vaijayanti A.,Ganesh, Krishna N.

, p. 3085 - 3088 (2007/10/03)

The design and facile synthesis of a novel chiral six-membered PNA analogue (2S,5R )-1-(N-Boc-aminoethyl)-5-(thymin-1-yl)pipecolic acid, aepipPNA, that upon incorporation into PNA sequences effected stabilization of complexes with target complementary DNA

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