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3-amino-5-phenylthieno[2,3-d]pyrimidin-4(3H)-one is a heterocyclic compound characterized by a thienopyrimidine core, which consists of a thiophene ring fused to a pyrimidine ring. The molecule features an amino group at the 3-position and a phenyl group at the 5-position, which are key to its chemical properties and potential applications. 3-amino-5-phenylthieno[2,3-d]pyrimidin-4(3H)-one is of interest in medicinal chemistry, particularly in the development of new drugs, due to its ability to form hydrogen bonds and its potential to interact with various biological targets. The specific arrangement of the amino and phenyl groups can influence its binding affinity and selectivity, making it a promising candidate for further investigation in drug discovery and development.

5628-27-3

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5628-27-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5628-27-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,2 and 8 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5628-27:
(6*5)+(5*6)+(4*2)+(3*8)+(2*2)+(1*7)=103
103 % 10 = 3
So 5628-27-3 is a valid CAS Registry Number.

5628-27-3SDS

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 calcium,5-ethyl-4,6-dioxo-5-propan-2-yl-1H-pyrimidin-2-olate

1.2 Other means of identification

Product number -
Other names Probarbital calcium

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:5628-27-3 SDS

5628-27-3Relevant academic research and scientific papers

Synthesis of Bipyridyl-, Viologen-, and Quinone-bridged Porphyrins

Leighton, Philip,Sanders, Jeremy K. M.

, p. 2385 - 2394 (2007/10/02)

Mesoporphyrin-II has been bridged by several 2,2'-hydroxymethyl-substituted 4,4'-bipyridine compounds.N-Methylation of the bipyridine bridge groups yielded viologen-bridged porphyrins which have unusual aggregation and fluorescence properties.An improved route to quinone-bridged porphyrins is also reported.

Quinone-capped Porphyrins: Synthesis and some Chemical Properties

Ganesh, K. Nagappa,Sanders, Jeremy K. M.

, p. 1611 - 1616 (2007/10/02)

The 2,5-bis(hydroxyethyl) and 2,5-bis(hydroxypropyl) derivatives of hydroquinone bis(methoxymethyl) ether have been synthesised and used to 'cap' mesoporphyrin-II.Deprotection, oxidation, and metallation gave the title compounds.Several anomalous reactivi

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