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1,4-Piperidinedicarboxylic acid, 4-aMino-, 4-Methyl 1-(phenylMethyl) ester is a chemical compound derived from piperidinedicarboxylic acid, featuring a methyl group and a phenylmethyl ester group attached to the 4-amine position. 1,4-Piperidinedicarboxylic acid, 4-aMino-, 4-Methyl 1-(phenylMethyl) ester is utilized as a raw material in the synthesis of pharmaceutical drugs and research chemicals, and it holds potential in medicinal chemistry and drug development due to its capacity to modulate various biological pathways and processes. Careful handling is advised due to potential hazards associated with its use.

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  • 1,4-Piperidinedicarboxylic acid, 4-amino-, 4-Methyl 1-(phenylmethyl) ester

    Cas No: 115655-42-0

  • USD $ 1.9-2.9 / Gram

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  • 115655-42-0 Structure
  • Basic information

    1. Product Name: 1,4-Piperidinedicarboxylic acid, 4-aMino-, 4-Methyl 1-(phenylMethyl) ester
    2. Synonyms: 1,4-Piperidinedicarboxylic acid, 4-aMino-, 4-Methyl 1-(phenylMethyl) ester;O1-Benzyl O4-methyl 4-aminopiperidine-1,4-dicarboxylate
    3. CAS NO:115655-42-0
    4. Molecular Formula: C15H21N2O4
    5. Molecular Weight: 293.33824
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 115655-42-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,4-Piperidinedicarboxylic acid, 4-aMino-, 4-Methyl 1-(phenylMethyl) ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,4-Piperidinedicarboxylic acid, 4-aMino-, 4-Methyl 1-(phenylMethyl) ester(115655-42-0)
    11. EPA Substance Registry System: 1,4-Piperidinedicarboxylic acid, 4-aMino-, 4-Methyl 1-(phenylMethyl) ester(115655-42-0)
  • 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: 115655-42-0(Hazardous Substances Data)

115655-42-0 Usage

Uses

Used in Pharmaceutical Industry:
1,4-Piperidinedicarboxylic acid, 4-aMino-, 4-Methyl 1-(phenylMethyl) ester is used as a raw material for the synthesis of pharmaceutical drugs, leveraging its ability to influence biological pathways and processes to contribute to the development of new medications.
Used in Research Chemicals:
In the field of research, this compound serves as a key component in the synthesis of various research chemicals, facilitating the exploration of its properties and potential applications in drug discovery and medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 115655-42-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,6,5 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 115655-42:
(8*1)+(7*1)+(6*5)+(5*6)+(4*5)+(3*5)+(2*4)+(1*2)=120
120 % 10 = 0
So 115655-42-0 is a valid CAS Registry Number.

115655-42-0Downstream Products

115655-42-0Relevant articles and documents

With the biological activity of the 1, 3, 8 - triazaspiro [4, 5] decane - 2 - guanidine - 4 - ketone compound and its preparation method and application

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Paragraph 0022; 0023, (2017/08/25)

The present invention discloses a 1,3,8-triazaspiro[4,5]decane-2-guanidine-4-ketone compound with biological activity, a preparation method therefor and application thereof, and belongs to the technical field of pesticide synthesis. A technical solution of the present invention is that: the 1,3,8-triazaspiro[4,5]decane-2-guanidine-4-ketone compound with biological activity has the formula shown in the specification, wherein R is ethyl, propyl, isopropyl or phenyl. The present invention also discloses a preparation method of the 1,3,8-triazaspiro[4,5]decane-2-guanidine-4-ketone compound with biological activity, and application thereof in preparing pesticides. According to the invention, by a new method, a series of 1,3,8-triazaspiro[4,5]decane-2-guanidine-4-ketone compounds with biological activity are synthesized. The invention has the advantages of simple and easy operation in a reaction process, easy access to cheap raw materials, higher reaction efficiency, better repeatability, and remarkable bioactive effects, and has better prospects for application in the field of pesticide preparation.

INHIBITORS OF UNDECAPRENYL PYROPHOSPHATE SYNTHASE

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Page/Page column 145; 146, (2008/06/13)

The present invention relates to compounds that are selective and/or potent inhibitors of UPPS. In addition to compounds which inhibit UPPS, the invention also provides pharmaceutical compositions comprising these compounds and methods of using these comp

Heptanoyl-glu-asp-ala-amino acid immunostimulants

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, (2008/06/13)

Peptides useful as antiinfective agents, immunomodulators for stimulation of host defenses in patients with an increased risk of bacterial infections, intermediates and process therefor.

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