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145100-54-5

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145100-54-5 Usage

General Description

BENZYL 2-N-PROPYL-4-OXO-3,4-DIHYDROPYRIDINE-1(2H)-CARBOXYLATE is a chemical compound with a complex molecular structure. It is a dihydropyridine derivative, which means it contains a six-membered ring with two double bonds and a ketone group. The compound also contains a benzyl group, a propyl group, and a carboxylate group, which all contribute to its overall chemical properties. BENZYL 2-N-PROPYL-4-OXO-3,4-DIHYDROPYRIDINE-1(2H)-CARBOXYLATE may have potential applications in pharmaceuticals or organic synthesis due to its unique structure and potential biological activity. Further research and study may be needed to fully understand its potential uses and effects.

Check Digit Verification of cas no

The CAS Registry Mumber 145100-54-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,1,0 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 145100-54:
(8*1)+(7*4)+(6*5)+(5*1)+(4*0)+(3*0)+(2*5)+(1*4)=85
85 % 10 = 5
So 145100-54-5 is a valid CAS Registry Number.

145100-54-5SDS

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 benzyl 4-oxo-2-propyl-2,3-dihydropyridine-1-carboxylate

1.2 Other means of identification

Product number -
Other names -

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:145100-54-5 SDS

145100-54-5Relevant articles and documents

Highly Enantioselective Catalytic Addition of Grignard Reagents to N-Heterocyclic Acceptors

Guo, Yafei,Harutyunyan, Syuzanna R.

, p. 12950 - 12954 (2019/08/07)

General methods to prepare chiral N-heterocyclic molecular scaffolds are greatly sought after because of their significance in medicinal chemistry. Described here is the first general catalytic methodology to access a wide variety of chiral 2- and 4-substituted tetrahydro-quinolones, dihydro-4-pyridones, and piperidones with excellent yields and enantioselectivities, utilizing a single catalyst system.

C-3 acetoxylation of N-acyl-2,3-dihydro-4-pyridones

Comins, Daniel L.,Stolze, David A.,Thakker, Paresh,McArdle, Cheryl L.

, p. 5693 - 5696 (2007/10/03)

Stereoselective acetoxylation at the C-3 position of N-acyl-2-alkyl- 2,3-dihydro-4-pyridones was effected with Pb(OAc)4 in refluxing toluene.

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