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82859-02-7

(4,5,6,7-TETRAHYDRO-1H-PYRROLO[3,2-C]PYRIDIN-4-YL)-ACETIC ACID ETHYL ESTER is a chemical compound belonging to the class of pyrrolopyridine derivatives. It is characterized by its diverse pharmacological activities and potential applications in the treatment of central nervous system disorders.

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  • (4,5,6,7-TETRAHYDRO-1H-PYRROLO[3,2-C]PYRIDIN-4-YL)-ACETIC ACID ETHYL ESTER

    Cas No: 82859-02-7

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  • 82859-02-7 Structure

  • Basic information

    1. Product Name: (4,5,6,7-TETRAHYDRO-1H-PYRROLO[3,2-C]PYRIDIN-4-YL)-ACETIC ACID ETHYL ESTER
    2. Synonyms: (4,5,6,7-TETRAHYDRO-1H-PYRROLO[3,2-C]PYRIDIN-4-YL)-ACETIC ACID ETHYL ESTER
    3. CAS NO:82859-02-7
    4. Molecular Formula: C11H16N2O2
    5. Molecular Weight: 208.26
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 82859-02-7.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: (4,5,6,7-TETRAHYDRO-1H-PYRROLO[3,2-C]PYRIDIN-4-YL)-ACETIC ACID ETHYL ESTER(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4,5,6,7-TETRAHYDRO-1H-PYRROLO[3,2-C]PYRIDIN-4-YL)-ACETIC ACID ETHYL ESTER(82859-02-7)
    11. EPA Substance Registry System: (4,5,6,7-TETRAHYDRO-1H-PYRROLO[3,2-C]PYRIDIN-4-YL)-ACETIC ACID ETHYL ESTER(82859-02-7)

  • 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: 82859-02-7(Hazardous Substances Data)

82859-02-7 Usage

Uses

Used in Pharmaceutical Industry:
(4,5,6,7-TETRAHYDRO-1H-PYRROLO[3,2-C]PYRIDIN-4-YL)-ACETIC ACID ETHYL ESTER is used as a potential drug candidate for its interactions with various biological targets, including neurotransmitter receptors. This makes it a valuable compound in the development of treatments for central nervous system disorders.
Used in Medicinal Chemistry Research:
(4,5,6,7-TETRAHYDRO-1H-PYRROLO[3,2-C]PYRIDIN-4-YL)-ACETIC ACID ETHYL ESTER is used as a valuable chemical in medicinal chemistry research due to its diverse pharmacological activities and potential for drug development.
Used in Drug Formulation:
The ethyl ester form of (4,5,6,7-TETRAHYDRO-1H-PYRROLO[3,2-C]PYRIDIN-4-YL)-ACETIC ACID ETHYL ESTER is used to improve the solubility and bioavailability of the compound, which can be beneficial in the formulation of drugs targeting central nervous system disorders.

Check Digit Verification of cas no

The CAS Registry Mumber 82859-02-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,8,5 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 82859-02:
(7*8)+(6*2)+(5*8)+(4*5)+(3*9)+(2*0)+(1*2)=157
157 % 10 = 7
So 82859-02-7 is a valid CAS Registry Number.

82859-02-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-carbethoxymethyl-4,5,6,7-tetrahydro[1H]pyrrolo[3,2-c]pyridine

1.2 Other means of identification

Product number -
Other names (4,5,6,7-TETRAHYDRO-1H-PYRROLO[3,2-C]PYRIDIN-4-YL)-ACETIC ACID ETHYL 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:82859-02-7 SDS

82859-02-7Relevant articles and documents

Synthesis in the Diazasteroid Group. XVIII. Syntheses of the 9,17-Diazasteroid System

Matoba, Katsuhide,Fukushima, Akiko,Takahata, Hiroki,Hirai, Yoshiro,Yamazaki, Takao

, p. 1300 - 1306 (2007/10/02)

A 9,17-diazasteroid system, I, was synthesized from an aminoester, III, and cyclohexanone.Unfortunately the yield was poor.Another 9,17-diazasteroid system, II, was prepared from the condensation product, XVa, of quinoline N-oxide with an active methine compound, IV.Thus, XVa was hydrolyzed, followed by decarboxylation, reduction and cyclization.The yield in each step to II was moderate.Keywords- azasteroid; diazasteroid; quinoline N-oxide; cyclization; Pictet-Spengler reaction; active methylene compound; pyrrolopyridine; quinolylpyrrolidine

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