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Methyl 3-amino-1-benzylpyrrolidine-3-Carboxylate is a versatile chemical compound with the molecular formula C15H20N2O2. It is a pyrrolidine derivative characterized by the presence of a methyl ester, an amino group, and a benzyl group. Methyl 3-amino-1-benzylpyrrolidine-3-Carboxylate holds promise in the realms of organic synthesis and medicinal chemistry, attributed to its valuable pharmaceutical properties.

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  • 3-Pyrrolidinecarboxylicacid, 3-amino-1-(phenylmethyl)-, methyl ester

    Cas No: 145602-88-6

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  • 145602-88-6 Structure
  • Basic information

    1. Product Name: Methyl 3-amino-1-benzylpyrrolidine-3-Carboxylate
    2. Synonyms: Methyl 3-amino-1-benzylpyrrolidine-3-Carboxylate
    3. CAS NO:145602-88-6
    4. Molecular Formula: C13H18N2O2
    5. Molecular Weight: 234.29
    6. EINECS: 604-604-1
    7. Product Categories: N/A
    8. Mol File: 145602-88-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 319.6 °C at 760 mmHg
    3. Flash Point: 147.1 °C
    4. Appearance: /
    5. Density: 1.161 g/cm3
    6. Vapor Pressure: 0.000336mmHg at 25°C
    7. Refractive Index: 1.563
    8. Storage Temp.: 2-8°C(protect from light)
    9. Solubility: N/A
    10. CAS DataBase Reference: Methyl 3-amino-1-benzylpyrrolidine-3-Carboxylate(CAS DataBase Reference)
    11. NIST Chemistry Reference: Methyl 3-amino-1-benzylpyrrolidine-3-Carboxylate(145602-88-6)
    12. EPA Substance Registry System: Methyl 3-amino-1-benzylpyrrolidine-3-Carboxylate(145602-88-6)
  • 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: 145602-88-6(Hazardous Substances Data)

145602-88-6 Usage

Uses

Used in Organic Synthesis:
Methyl 3-amino-1-benzylpyrrolidine-3-Carboxylate is utilized as a key intermediate in organic synthesis for the preparation of various complex organic molecules. Its unique structural features, including the amino and benzyl groups, facilitate its use in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, Methyl 3-amino-1-benzylpyrrolidine-3-Carboxylate serves as a building block for the development of novel therapeutic agents. Its ability to form stable covalent bonds with biological targets makes it a promising candidate for the design of drugs targeting specific receptors or enzymes.
Used in Pharmaceutical Industry:
Methyl 3-amino-1-benzylpyrrolidine-3-Carboxylate is employed as an active pharmaceutical ingredient (API) in the development of new drugs. Its unique chemical structure allows for the modulation of biological activity, making it suitable for the treatment of various diseases and disorders.
Used in Drug Delivery Systems:
Methyl 3-amino-1-benzylpyrrolidine-3-Carboxylate can be incorporated into drug delivery systems to improve the pharmacokinetics and pharmacodynamics of therapeutic agents. Its compatibility with various polymers and materials enables the development of targeted drug delivery systems, enhancing the efficacy and safety of medications.
Used in Chemical Research:
In the realm of chemical research, Methyl 3-amino-1-benzylpyrrolidine-3-Carboxylate is utilized as a model compound for studying various chemical reactions and mechanisms. Its reactivity and structural features provide valuable insights into the behavior of similar compounds and contribute to the advancement of chemical knowledge.

Check Digit Verification of cas no

The CAS Registry Mumber 145602-88-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,6,0 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 145602-88:
(8*1)+(7*4)+(6*5)+(5*6)+(4*0)+(3*2)+(2*8)+(1*8)=126
126 % 10 = 6
So 145602-88-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H18N2O2/c1-17-12(16)13(14)7-8-15(10-13)9-11-5-3-2-4-6-11/h2-6H,7-10,14H2,1H3

145602-88-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 3-amino-1-benzylpyrrolidine-3-carboxylate

1.2 Other means of identification

Product number -
Other names Methyl 3-amino-1-benzylpyrrolidine-3-Carboxylate

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:145602-88-6 SDS

145602-88-6Relevant articles and documents

G protein coupled receptor agonist and application thereof in treatment of diabetes

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Paragraph 0017; 0018, (2018/06/16)

The invention discloses a structure of a compound. The structural formula of the compound is shown in the description. Found by activity determination, the structure has the effect of a G protein coupled receptor 119 agonist; the G protein coupled receptor 119 agonist has the functions of not causing hypoglycemia of patients and promoting GLP-1 secretion. The compound disclosed by the invention can be further researched and developed as a diabetes-resisting drug. Besides, the invention further discloses a synthesis route and a synthesis method for the compound.

SPIRO-CONDENSED PYRROLIDINE DERIVATIVES AS DEUBIQUITYLATING ENZYMES (DUB) INHIBITORS

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Page/Page column 45-47, (2017/09/15)

The present invention relates to novel compounds and methods for the manufacture of inhibitors of deubiquitylating enzymes (DUBs). In particular, the invention relates to the inhibition of Cezanne 1. The invention further relates to the use of DUB inhibitors in the treatment of cancer. (Figure (I))

INHIBITORS OF FACTOR XA AND OTHER SERINE PROTEASES INVOLVED IN THE COAGULATION CASCADE

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Page 86-87, (2010/02/06)

This invention discloses amino acid derivatives which display inhibitory effects on the serine protease factor Xa. The invention also discloses pharmaceutically acceptable salts of the compounds, pharmaceutically acceptable compositions comprising the compounds or their salts, methods for the preparation of the compounds, and methods of using them as therapeutic agents for treating or preventing disease states in mammals characterized by abnormal thrombosis.

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