Welcome to LookChem.com Sign In|Join Free
  • or
1-(2,2-Dimethoxyethyl)-1,6-dihydro-6-oxo-2-phenyl-5-pyrimidinecarboxylic acid methyl ester is a methyl ester derivative of a pyrimidinecarboxylic acid, featuring a dihydro-6-oxo-2-phenyl-5-pyrimidine ring with a carboxylic acid group and a methyl ester group. It also has a 2,2-dimethoxyethyl substituent attached to the pyrimidine ring, which may contribute to its potential biological and pharmacological activities.

308276-58-6

Post Buying Request

308276-58-6 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

308276-58-6 Usage

Uses

Used in Pharmaceutical Industry:
1-(2,2-Dimethoxyethyl)-1,6-dihydro-6-oxo-2-phenyl-5-pyrimidinecarboxylic acid methyl ester is used as a potential drug candidate for targeting pyrimidine metabolism, due to its unique chemical structure and the presence of the pyrimidine ring.
Used in Drug Synthesis:
In the pharmaceutical industry, 1-(2,2-Dimethoxyethyl)-1,6-dihydro-6-oxo-2-phenyl-5-pyrimidinecarboxylic acid methyl ester is used as a starting material for the synthesis of other pyrimidine-based compounds, which may have various therapeutic applications.
Used in Research and Development:
Due to its chemical structure and potential biological and pharmacological activities, 1-(2,2-Dimethoxyethyl)-1,6-dihydro-6-oxo-2-phenyl-5-pyrimidinecarboxylic acid methyl ester is used as a subject of interest for further research and development in the fields of medicinal chemistry and drug discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 308276-58-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,8,2,7 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 308276-58:
(8*3)+(7*0)+(6*8)+(5*2)+(4*7)+(3*6)+(2*5)+(1*8)=146
146 % 10 = 6
So 308276-58-6 is a valid CAS Registry Number.

308276-58-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 1-(2,2-dimethoxyethyl)-6-oxo-2-phenylpyrimidine-5-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:308276-58-6 SDS

308276-58-6Relevant academic research and scientific papers

HERBICIDAL BIS-NITROGEN-CONTAINING OXO HETEROCYCLES

-

, (2012/09/22)

Disclosed are compounds of Formula 1, including all stereoisomers, N oxides, and salts thereof, A is a radical selected from the group consisting of, and B1, B2, B3, T, R1, R2 R3, R4, R5, R6, R7, R8, R9, R10, R11, R12 and R13 are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula 1 and methods for controlling undesired vegetation comprising contacting the undesired vegetation or its environment with an effective amount of a compound or a composition of the invention.

Nonpeptidic inhibitors of human leukocyte elastase. 5. Design, synthesis, and X-ray crystallography of a series of orally active 5-aminopyrimidin-6- one-containing trifluoromethyl ketones

Veale,Bernstein,Bryant,Ceccarelli,Damewood Jr.,Earley,Feeney,Gomes,Kosmider,Steelman,Thomas,Vacek,Williams,Wolanin,Woolson

, p. 98 - 108 (2007/10/02)

The effects of changes in substitution in a series of 5-amino-2- pyrimidin-6-ones on both in vitro activity and oral activity in an acute hemorrhage assay have been explored. These compounds contained either a trifluoromethyl ketone or a boronic acid moiety to bind covalently to the Ser-195 hydroxyl of human leukocyte elastase (HLE). Boronic acid-containing inhibitors were found to be more potent than the corresponding trifluoromethyl ketones in vitro but were less active upon oral administration. Compound 13b was found to offer the best combination of oral potency, duration of action, and enzyme selectivity and, as such, was selected for further biological testing. X-ray crystallography of a cocrystallized complex of compound 19m and porcine pancreatic elastase demonstrated that the inhibitor is bound to the enzyme in a manner similar to that found previously for a closely related series of pyridone-containing inhibitors of HLE.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 308276-58-6