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(2R-trans)-5-Hydroxy-1,2-piperidinedicarboxylic acid 2-methyl 1-benzyl ester is a chiral chemical compound with the molecular formula C16H21NO5. It is an ester derivative of a piperidine carboxylic acid, featuring a hydroxy group at the 5-position, a methyl group at the 2-position, and a benzyl ester group attached to the carboxylic acid moiety. This unique structure and configuration may endow it with potential biological or pharmaceutical applications, although further research is required to explore its full potential.

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  • (2R-trans)-5-Hydroxy-1,2-piperidinedicarboxylic acid 2-methyl 1-benzyl ester

    Cas No: 133808-76-1

  • USD $ 1.9-2.9 / Gram

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  • 133808-76-1 Structure
  • Basic information

    1. Product Name: (2R-trans)-5-Hydroxy-1,2-piperidinedicarboxylic acid 2-methyl 1-benzyl ester
    2. Synonyms: (2R-trans)-5-Hydroxy-1,2-piperidinedicarboxylic acid 2-methyl 1-benzyl ester
    3. CAS NO:133808-76-1
    4. Molecular Formula: C15H19NO5
    5. Molecular Weight: 293.32
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 133808-76-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.272
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (2R-trans)-5-Hydroxy-1,2-piperidinedicarboxylic acid 2-methyl 1-benzyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2R-trans)-5-Hydroxy-1,2-piperidinedicarboxylic acid 2-methyl 1-benzyl ester(133808-76-1)
    11. EPA Substance Registry System: (2R-trans)-5-Hydroxy-1,2-piperidinedicarboxylic acid 2-methyl 1-benzyl ester(133808-76-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 133808-76-1(Hazardous Substances Data)

133808-76-1 Usage

Uses

Used in Pharmaceutical Industry:
(2R-trans)-5-Hydroxy-1,2-piperidinedicarboxylic acid 2-methyl 1-benzyl ester is used as a potential pharmaceutical candidate for various applications due to its unique structure and chiral configuration. Its specific biological activity and interactions with biological targets need to be investigated to determine its suitability for drug development.
Used in Research and Development:
In the field of chemical research, (2R-trans)-5-Hydroxy-1,2-piperidinedicarboxylic acid 2-methyl 1-benzyl ester serves as a subject for studying the synthesis, properties, and potential applications of chiral ester derivatives. Understanding its behavior and reactivity can contribute to the advancement of organic chemistry and the discovery of new compounds with therapeutic potential.

Check Digit Verification of cas no

The CAS Registry Mumber 133808-76-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,8,0 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 133808-76:
(8*1)+(7*3)+(6*3)+(5*8)+(4*0)+(3*8)+(2*7)+(1*6)=131
131 % 10 = 1
So 133808-76-1 is a valid CAS Registry Number.

133808-76-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-Benzyl 2-methyl (2R,5S)-5-hydroxy-1,2-piperidinedicarboxylate

1.2 Other means of identification

Product number -
Other names -

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

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More Details:133808-76-1 SDS

133808-76-1Relevant articles and documents

CHIRAL SYNTHESIS OF 5-HYDROXY-(L)-PIPECOLIC ACIDS FROM (L)-GLUTAMIC ACID

Bailey, Patrick D.,Bryans, Justin S.

, p. 2231 - 2234 (2007/10/02)

A stereo- and enantio-specific synthesis of the naturally occuring cis-5-hydroxy-(L)-pipecolic acid (3) is described, starting from Z-(L)-glutamic acid; the key step involves cyclisation of a protected chlorohydrin, and also gives access to trans-5-hydroxy-(L)-pipecolic acid.

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