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39658-41-8

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39658-41-8 Usage

General Description

Ethyl 6-aminonicotinate, also known as N-ethyl-6-aminonicotinate or Nicotinic acid, ethyl ester, 6-amino, is a synthetic compound characterized by its ethanol structure combined with a nicotinic acid that has been substituted with an amino group at position 6. It's an organic compound belonging to the pyridines class and its molecular formula is C8H10N2O2. It is generally used in scientific research and experimentations, particularly in the pharmaceutical industry for drug discovery and development. However, detailed information about its potential applications and safety in medical treatments is limited, requiring further studies and investigations.

Check Digit Verification of cas no

The CAS Registry Mumber 39658-41-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,6,5 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 39658-41:
(7*3)+(6*9)+(5*6)+(4*5)+(3*8)+(2*4)+(1*1)=158
158 % 10 = 8
So 39658-41-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H10N2O2/c1-2-12-8(11)6-3-4-7(9)10-5-6/h3-5H,2H2,1H3,(H2,9,10)/p+1

39658-41-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 2-Aminopyridine-5-carboxylate

1.2 Other means of identification

Product number -
Other names Ethyl 6-aminonicotinate

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:39658-41-8 SDS

39658-41-8Relevant articles and documents

Mild, General, and Regioselective Synthesis of 2-Aminopyridines from Pyridine N -Oxides via N -(2-Pyridyl)pyridinium Salts

Xiong, Hui,Hoye, Adam T.

supporting information, p. 371 - 375 (2022/01/27)

A synthesis of 2-aminopyridines from pyridine N-oxides via their corresponding N-(2-pyridyl)pyridinium salts has been demonstrated and investigated. The reaction sequence features a highly regioselective conversion of the N-oxide into its pyridinium salt

Sulfa drug haptens and its preparation method and application

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Paragraph 0020; 0022, (2017/08/26)

The invention discloses a hapten, and a preparation method and application thereof, particularly a sulfonamide hapten. The invention also discloses a preparation method and application of the hapten. The kit quick detection product established on the basi

ISOPROPYL TRIAZOLO PYRIDINE COMPOUNDS

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Page/Page column 11; 12, (2015/07/23)

The present invention provides a compound of the Formula (I) below: Wherein R1 is selected from the group consisting of H, CH3, CN, CH2CN, C(CH3)2CN, and F; R2 is selected from the group consisting of H, O(C1-C3alkyl)R5, CH2CN, and CN; R3 is selected from the group consisting of H, OCH3, CN, C(CH3)2CN, and CH2CN; R4 is selected from the group consisting of H and CH3; R5 is selected from the group consisting of H, CN, C(CH3)2CN, OCH3, S(O)2CH3, and C(CH3)2OH; provided that at least one selected from the group consisting of R1, R2, R3 and R4 is H; or a pharmaceutically acceptable salt thereof, methods of treating diabetes using the compound and a process for preparing the compound.

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