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CAS

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164077-50-3

3,5-Diethoxypyridine-4-carboxaldehyde is a chemical compound with the formula C11H13NO3, characterized by its yellow to brown liquid form and a faint but distinctive odor.
Used in Pharmaceutical Industry:
3,5-Diethoxypyridine-4-carboxaldehyde is used as an intermediate in the synthesis of pharmaceuticals for its versatile building block properties in organic synthesis, particularly in the production of heterocyclic compounds.
Used in Agrochemical Industry:
3,5-Diethoxypyridine-4-carboxaldehyde is used as an intermediate in the synthesis of agrochemicals, contributing to the development of various organic compounds for agricultural applications.
Used in Organic Synthesis:
3,5-Diethoxypyridine-4-carboxaldehyde is used as a versatile building block in organic synthesis, playing a crucial role in the creation of heterocyclic compounds.
Used in Medical Research:
3,5-Diethoxypyridine-4-carboxaldehyde is used as a subject of study for its potential anti-inflammatory and antiproliferative properties, indicating its interest for further medical research and development.

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  • 164077-50-3 Structure

  • Basic information

    1. Product Name: 3,5-Diethoxypyridine-4-carboxaldehyde
    2. Synonyms: 3,5-Diethoxypyridine-4-carboxaldehyde;3,5-Diethoxyisonicotinaldehyde
    3. CAS NO:164077-50-3
    4. Molecular Formula: C10H13NO3
    5. Molecular Weight: 195.22
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 164077-50-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 341.9±37.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.113±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. PKA: 2.22±0.10(Predicted)
    10. CAS DataBase Reference: 3,5-Diethoxypyridine-4-carboxaldehyde(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3,5-Diethoxypyridine-4-carboxaldehyde(164077-50-3)
    12. EPA Substance Registry System: 3,5-Diethoxypyridine-4-carboxaldehyde(164077-50-3)

  • 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: 164077-50-3(Hazardous Substances Data)

164077-50-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 164077-50-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,0,7 and 7 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 164077-50:
(8*1)+(7*6)+(6*4)+(5*0)+(4*7)+(3*7)+(2*5)+(1*0)=133
133 % 10 = 3
So 164077-50-3 is a valid CAS Registry Number.

164077-50-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-diethoxypyridine-4-carbaldehyde

1.2 Other means of identification

Product number -
Other names 3,5-Diethoxypyridine-4-carboxaldehyde

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:164077-50-3 SDS

164077-50-3Downstream Products

164077-50-3Relevant articles and documents

3,5-DICHLORO-4-PYRIDINECARBONITRILE AS A KEY REAGENT IN A SYNTHESIS OF COPPER CONTAINING AMINE OXIDASE INHIBITORS

Bertini, Vincenzo,Lucchesini, Francesco,Pocci, Marco,Munno, Angela De

, p. 675 - 688 (1995)

Various synthetic approaches to 3,4,5-trifunctionalized pyridine derivatives useful as benzylamine oxidase inhibitors are extensively explored.Fully satisfactory preparations of the inhibitors 3,5-diethoxy-4-aminomethylpyridine (4), 3,5-bis(3-hydroxypropoxy)-4-aminomethylpyridine (11), 3,5-bis(4-hydroxybutoxy)-4-aminomethylpyridine (12) and 3-ethoxy-5-phenylmethoxy-4-aminomethylpyridine (16), all in the form of dihydrochloride salt, using 3,5-dichloro-4-pyridinecarbonitrile as key precursor, are reported.

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