188782-68-5 Usage
Description
(3-amino-6-phenyl-4-(thiophen-2-yl)thieno[2,3-b]pyridin-2-yl)(phenyl)methanone is a complex organic chemical compound characterized by a thieno[2,3-b]pyridine core, which is fused with a thiophene ring and a phenyl ring. The molecule also features a phenylmethylketone group, contributing to its unique structure and potential reactivity. (3-amino-6-phenyl-4-(thiophen-2-yl)thieno[2,3-b]pyridin-2-yl)(phenyl)methanone may hold promise in various fields such as pharmaceuticals, materials science, and organic synthesis due to its distinctive molecular architecture.
Uses
Used in Pharmaceutical Industry:
(3-amino-6-phenyl-4-(thiophen-2-yl)thieno[2,3-b]pyridin-2-yl)(phenyl)methanone is used as a potential pharmaceutical agent for its unique molecular structure, which may offer novel therapeutic properties. Its potential applications could include the development of new drugs targeting specific biological pathways or receptors, pending further research and testing to confirm its bioactivity and safety.
Used in Materials Science:
In the field of materials science, (3-amino-6-phenyl-4-(thiophen-2-yl)thieno[2,3-b]pyridin-2-yl)(phenyl)methanone may be utilized as a component in the synthesis of new materials with specific properties, such as electronic, optical, or mechanical characteristics. Its incorporation into polymers or other composites could lead to advancements in material performance.
Used in Organic Synthesis:
As a complex chemical compound, (3-amino-6-phenyl-4-(thiophen-2-yl)thieno[2,3-b]pyridin-2-yl)(phenyl)methanone can be employed as a building block or intermediate in organic synthesis. It may be used to construct more complex molecules or to develop new synthetic routes to existing compounds, expanding the scope of chemical reactions and products available to researchers and industry professionals.
Check Digit Verification of cas no
The CAS Registry Mumber 188782-68-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,8,7,8 and 2 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 188782-68:
(8*1)+(7*8)+(6*8)+(5*7)+(4*8)+(3*2)+(2*6)+(1*8)=205
205 % 10 = 5
So 188782-68-5 is a valid CAS Registry Number.
188782-68-5Relevant articles and documents
Thienopyridine bis-heterocyclic compound preparation technology
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Paragraph 0007; 0019-0020, (2018/03/01)
The invention provides a thienopyridine bis-heterocyclic compound preparation technology which comprises the following steps: 1) putting acetophenone and thiophene-2-formaldehyde in an alcohol solventto react under the alkali action to obtain a compound II; 2) putting the compound II and 2-cyanoethyl thioacetamide in the alcohol solvent to react under the organic alkali action to obtain a compound III; 3) putting the compound III and bromoacetophenone in the alcohol solvent to react under the strong base action to obtain a compound I. A reaction route is shown in the specification. The preparation technology disclosed by the invention has the following advantages that the raw materials and reagents utilized by the reaction are all general synthesized reagents and has cheap price and easiness in obtaining; all the steps have moderate reaction conditions and simple aftertreatment operation; the reaction yield is higher, and the product purity is high; the whole preparation technology has the advantages of convenience in operation, low product cost and ability in meeting an industrial production requirement.
Reactions of styrylthienyl ketone, styryl furyl ketone with thiocyanoacetamide: Synthesis of several new pyridines, thieno[2,3-b]pyridines, pyrido [2′,3′:4,5]thieno[3,2-c]pyridazines and pyrido-[3′,2′:4,5]thieno[3,2-d]pyrimidin one derivatives
Attaby, Fawzy A.
, p. 1 - 12 (2007/10/03)
Styryl thienyl ketone and Styryl furyl ketone 2a,b reacted with thiocyanoacetamide(1) to give the dihydropyridinethiones 3a,b which used as starting material for the synthesis of several heterocyclic compounds. Reaction with several halogeno-esters, halogeno-ketones and chloroacetamide gave 2-S-alkoyl pyridines 5a-d, 10a-d, 13a,b and 19a,b thieno[2,3-c] pyridines 6a,b, 11a,b 14a,b and 20a-d, pyrido[2′,3′,4:5]thieno[2,3-c]pyridazines 8a,b and pyrido[2′.3′:-4,5]thieno[2,3-d]pyrimidinones 15a, b 16a,b and 17a,b. Structures were established based on elemental analyses and spectral data studies.
