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10230-58-7

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10230-58-7 Usage

Type of compound

Chemical compound

Derivative of

Nicotine

Pharmacological properties

Similar to nicotine

Industry use

Pharmaceutical industry

Application

Intermediate in the synthesis of various drugs

Research use

Different sources of media describe the Research use of 10230-58-7 differently. You can refer to the following data:
1. Studying effects on the nervous system
2. Precursor for the synthesis of other bioactive molecules

Potential

Development of new medications

Versatility

Various potential applications in medicine and research

Check Digit Verification of cas no

The CAS Registry Mumber 10230-58-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,2,3 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10230-58:
(7*1)+(6*0)+(5*2)+(4*3)+(3*0)+(2*5)+(1*8)=47
47 % 10 = 7
So 10230-58-7 is a valid CAS Registry Number.

10230-58-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Ethyl 1,2-dimethyl-6-oxo-1,4,5,6-tetrahydropyridine-3-carboxylate

1.2 Other means of identification

Product number -
Other names 1-Methyl-2-oxo-5-carbethoxy-6-methyl-1,2,3,4-tetrahydro-pyridin

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:10230-58-7 SDS

10230-58-7Downstream Products

10230-58-7Relevant articles and documents

ν-Triazolines. Part 36. New synthesis of ethyl 1-alkyl-1,4,5,6-tetrahydro-6-oxopyridine-3-carboxylates and 1-alkyl-1,4,5,6-tetrahydro-6-oxopyridine-3-carbonitriles through reduction of N-2-nitroarylamidines

Angelini, Roberto,Erba, Emanuela,Pocar, Donato

, p. 837 - 840 (2007/10/03)

Ethyl 1-alkyl-1,4-dihydropyridine-3-carboxylates 2a-d and 1-alkyl-1,4-dihydropyridine-3-carbonitriles 2e,f were allowed to react with 2-nitrophenyl azide 3 to give tertiary amidines 4 by spontaneous rearrangement of the triazoline cycloadducts. Ready catalytic hydrogenation with Pd-C of 4 gave the corresponding ethyl 1-alkyl-6-oxo-1,4,5,6-tetrahydropyridine-3-carboxylates 5a-d and 1-alkyl-6-oxo-1,4,5,6-tetrahydropyridine-3-carbonitriles 5e,f.

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