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889656-83-1

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889656-83-1 Usage

Molecular structure

1H-Pyrano[3,4-c]pyridine-5-carbonitrile features a complex structure with a pyrano-pyridine ring system and various functional groups attached.

Carbonitrile group

The compound has a carbonitrile (CN) group attached, which is a cyano group consisting of a carbon atom triple-bonded to a nitrogen atom.

Tetrahydro structure

The compound has a tetrahydro structure, meaning four hydrogen atoms are attached to the ring, contributing to its stability.

Dimethyl group

The compound contains a dimethyl (CH3) group, which consists of two methyl groups attached to the same carbon atom.

Thioxo group

The presence of a thioxo (C=S) group, which is a sulfur analog of an oxo group, adds to the compound's reactivity and chemical properties.

8th position substitution

The compound's eighth position is substituted with a methyl(phenylmethyl)amino group, which is a bulky, basic group that can influence the compound's solubility, stability, and interactions with other molecules.

Potential applications

Due to its intricate structure and multiple functional groups, 1H-Pyrano[3,4-c]pyridine-5-carbonitrile, 3,4,6,7-tetrahydro-3,3-dimethyl-8-[methyl(phenylmethyl)amino]-6-thioxois suitable for various chemical and biological applications, such as pharmaceutical and agrochemical research.

Check Digit Verification of cas no

The CAS Registry Mumber 889656-83-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,9,6,5 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 889656-83:
(8*8)+(7*8)+(6*9)+(5*6)+(4*5)+(3*6)+(2*8)+(1*3)=261
261 % 10 = 1
So 889656-83-1 is a valid CAS Registry Number.

889656-83-1Relevant articles and documents

NEW PYRIDO[3',2':4,5]FURO[3,2-d]PYRIMIDINE DERIVATIVES

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Page/Page column 36, (2010/11/25)

The present invention provides a pyridofuropyrimidine derivative of formula (I): wherein G1 represents a group selected from -CR6R7- and -O- wherein R6 and R7 independently represent hydrogen atoms or C1-4 alkyl groups; R1 and R2 are independently selected from hydrogen atoms and C1-4 alkyl groups; R3 represents a group selected from C1-4 alkyl, C1-4 alkoxy, amino, hydroxy, mono- C1-4 alkylamino, di- C1-4 alkylamino, C3-8 cycloalkylamino, aryl, heteroaryl and saturated N-containing heterocyclyl groups which are bound to the pyridine ring through their nitrogen atom, all of them being optionally substituted by one or more substituents selected from the group consisting of halogen atoms and hydroxy, C1-4 alkyl, C1-4 alkoxy- C1-4 alkyl, aryl-C1-4 4alkyl, -O(CO)O R8, C1-4 alkoxy, -(CO)NR8R9, -CN, -CF3, -NR8R9, -SR8 and -SO2NH2 groups wherein R8 and R9 each independently represent a hydrogen atom or a C1-4 alkyl group; R4 and R5 are independently selected from the group consisting of hydrogen atoms, C1-4 alkyl groups, hydroxyl- C1-4 alkyl groups and groups of formula (II): wherein p and q are integers selected from 0, 1 , 2 and 3; A is either a direct bond or a group selected from -CONR14-, -NR14CO-, -0-, -COO-, -OCO-, -S-, -SO- and -SO2-, wherein each R10, R11, R12, R13 and R14 independently represents a hydrogen atom or a C1-4 alkyl group and G2 is a group selected from aryl, heteroaryl or heterocyclyl groups; wherein the group G2 is optionally substituted by one or more substituents selected from group consisting of halogen atoms and C1-4 alkyl, hydroxy, oxo, C1-4 alkoxy- C1-4 alkyl, aryl- C1-4 alkyl, -(CO)OR16, C1-4 alkoxy, -(CO)NR16R17, -CN, -CF3, -NR16R17, -SR16 and -SO2NH2 groups; wherein R16 and R17 each independently represent a hydrogen atom or a C1-4 alkyl group and the pharmaceutically acceptable salts and N-oxides thereof.

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