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4-Ethyl-pyridine-2-carboxylic Acid, Hydrochloride is an off-white solid that serves as a valuable starting material in the synthesis of various pharmaceutical compounds, particularly Clindamycin analogues like Pirlimycin.

79415-18-2

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79415-18-2 Usage

Uses

Used in Pharmaceutical Industry:
4-Ethyl-pyridine-2-carboxylic Acid, Hydrochloride is used as a starting material for the synthesis of Clindamycin analogues, such as Pirlimycin, due to its chemical properties that facilitate the creation of these important antibiotics. These analogues are essential in the development of new drugs to combat bacterial infections, especially those resistant to existing treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 79415-18-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,4,1 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 79415-18:
(7*7)+(6*9)+(5*4)+(4*1)+(3*5)+(2*1)+(1*8)=152
152 % 10 = 2
So 79415-18-2 is a valid CAS Registry Number.

79415-18-2SDS

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 4-ethylpyridine-2-carboxylic acid,hydrochloride

1.2 Other means of identification

Product number -
Other names 2-Pyridinecarboxylic acid,4-ethyl-,hydrochloride

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:79415-18-2 SDS

79415-18-2Relevant academic research and scientific papers

An Improved Synthesis of Homoproline and Derivatives

Shuman, Robert T.,Ornstein, Paul L.,Paschal, Jonathan W.,Gesellchen, Paul D.

, p. 738 - 741 (2007/10/02)

An improved, general synthesis of substituted homoprolines has been developed by using readily available substituted pyridines (1).A key step in this synthetic procedure involves the known conversion of pyridine-N-oxides to 2-cyanopyridines (3) in nearly quantitative yields.The resulting nitriles are hydrolyzed to the corresponding pyridine-2-carboxylic acids (4).Subsequent reduction of the aromatic ring with PtO2/H2 gives the homoprolines (5) in good yields as racemic cis isomers.This procedure also can be utilized for the preparation of 5,6-benzohomoprolines fromthe appropriate quinoline precursors.The N-tert-butyloxycarbonyl (Boc) derivatives of these amino acids (useful intermediates for peptide synthesis) were also prepared in good yields.

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