700844-09-3 Usage
Uses
Used in Pharmaceutical Industry:
7-Chlorothieno[3,2-b]pyridine-6-carbonitrile is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure and properties contribute to the development of new drugs with improved therapeutic effects and reduced side effects.
Used in Agrochemical Industry:
In the agrochemical industry, 7-Chlorothieno[3,2-b]pyridine-6-carbonitrile serves as a crucial building block for the production of agrochemicals, such as pesticides and herbicides. Its incorporation into these compounds enhances their effectiveness in controlling pests and weeds, thereby improving crop yields and quality.
Used in Material Science:
7-Chlorothieno[3,2-b]pyridine-6-carbonitrile has potential applications in the field of material science due to its unique electronic properties. It can be used in the development of advanced materials with specific properties, such as conductivity, stability, and reactivity, which can be utilized in various applications, including sensors, catalysts, and energy storage devices.
Used in Organic Electronics:
The electronic properties of 7-Chlorothieno[3,2-b]pyridine-6-carbonitrile also make it a promising candidate for use in the field of organic electronics. It can be incorporated into organic electronic devices, such as organic light-emitting diodes (OLEDs), organic solar cells, and organic field-effect transistors (OFETs), to improve their performance and efficiency.
Used as a Building Block for Organic Molecules:
7-Chlorothieno[3,2-b]pyridine-6-carbonitrile is used as a versatile building block for the production of various organic molecules. Its unique structure allows for the synthesis of a wide range of compounds with diverse applications, including pharmaceuticals, agrochemicals, and materials for electronic devices.
Check Digit Verification of cas no
The CAS Registry Mumber 700844-09-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,0,8,4 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 700844-09:
(8*7)+(7*0)+(6*0)+(5*8)+(4*4)+(3*4)+(2*0)+(1*9)=133
133 % 10 = 3
So 700844-09-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H3ClN2S/c9-7-5(3-10)4-11-6-1-2-12-8(6)7/h1-2,4H
700844-09-3Relevant academic research and scientific papers
FUSED MULTICYCLIC COMPOUNDS AS PROTEIN KINASE INHIBITORS
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Page/Page column 55, (2010/04/25)
Fused multicyclic compounds of formula (I): wherein R′, R″, X, Y, Z, A, B, C, D, and n are defined herein. Also disclosed are a method for inhibiting protein kinase (e.g., Aurora kinase) activity and a method for treating a protein kinase mediated disorde
Thieno[3,2-b]pyridine-6-carbonitriles and thieno[2,3-b]pyridine-5-carbonitriles as protein kinase inhibitors
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, (2008/06/13)
This invention provides compounds of Formula (1a)-(1f), II wherein: X, m, n, q, R1, R2, R3, R4, R5, R6, R7, R8, R9, Y, Q, Z, Z′, Z′″, Z″ and J are defined hereinbefore in the specification, which are useful in the treatment of cancer, stroke, myocardial infarction, neuropathic pain, osteoporosis, polycystic kidney disease, autoimmune disease, rheumatoid arthritis, and transplant rejection and process for producing said compounds.
THIENO[3,2-b]PYRIDINE-6-CARBONITRILES AND THIENO[2,3-b]PYRIDINE-5-CARBONITRILES AS PROTEIN KINASE INHIBITORS
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Page 75, (2010/02/07)
This invention provides compounds of Formula (1 a) - (1f) wherein:X, R1, and R2 are defined hereinbefore in the specification, which are useful in the treatment of cancer, stroke, osteoporosis, polycystic kidney disease, autoimmune disease, rheumatoid arthritis, and transplant rejection and process for producing said compounds.
Identification of 7-phenylaminothieno-[3,2-b]pyridine-6-carbonitriles as a new class of Src kinase inhibitors
Boschelli, Diane H.,Wu, Biqi,Sosa, Ana Carolina Barrios,Durutlic, Haris,Ye, Fei,Raifeld, Yuri,Golas, Jennifer M.,Boschelli, Frank
, p. 6666 - 6668 (2007/10/03)
We disclose here a new class of kinase inhibitors, obtained by replacing the phenyl ring of a 3-quinolinecarbonitrile system with a thiophene ring. When suitably substituted, the resultant 7-phenylaminothieno[3,2-b]pyridine-6- carbonitrile analogues show
