Cas 313350-24-2,Carbamic acid, [4-(2-phenyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-, 1,1-dimethylethyl ester

313350-24-2

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Basic information

Product Name: Carbamic acid, [4-(2-phenyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-, 1,1-dimethylethyl ester
Synonyms:
CAS NO:313350-24-2
Molecular Formula: C25H28N4O2
Molecular Weight: 416.523
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Carbamic acid, [4-(2-phenyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-, 1,1-dimethylethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Carbamic acid, [4-(2-phenyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-, 1,1-dimethylethyl ester(313350-24-2)
EPA Substance Registry System: Carbamic acid, [4-(2-phenyl-1H-imidazo[4,5-c]quinolin-1-yl)butyl]-, 1,1-dimethylethyl ester(313350-24-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 313350-24-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 313350-24-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,3,3,5 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 313350-24:
(8*3)+(7*1)+(6*3)+(5*3)+(4*5)+(3*0)+(2*2)+(1*4)=92
92 % 10 = 2
So 313350-24-2 is a valid CAS Registry Number.

313350-24-2Upstream product

313350-24-2Downstream Products

313350-25-3 1-[4-(tert-butylcarbamyl)butyl]-2-phenyl-1H-imidazo[4,5-c]quinoline-5N-oxide

313350-24-2Relevant academic research and scientific papers

Sulfonamide and sulfamide substituted imidazoquinolines

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Page/Page column 25, (2010/02/05)

Imidazoquinoline and tetrahydroimidazoquinoline compounds that contain sulfonamide or sulfonamide functionality at the 1-position are useful as immune response modifiers. The compounds and compositions of the invention can induce the biosynthesis of vario

Amide substituted imidazoquinolines

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, (2008/06/13)

Imidazoquinoline and tetrahydroimidazoquinoline compounds that contain amide functionality at the 1-position are useful as immune response modifiers. The compounds and compositions of the invention can induce the biosynthesis of various cytokines and are useful in the treatment of a variety of conditions including viral diseases and neoplastic diseases.

Sulfonamide and sulfamide substituted imidazoquinolines and methods for the treatment of periodontal disease using these and other immune response modifiers

-

, (2008/06/13)

The disclosure provides methods for the treatment and prevention of periodontal disease. In preferred embodiments, the invention provides for local treatment of periodontal tissues with a pharmaceutical composition including an immune response modifier (I

Amide substituted imidazoquinolines

-

, (2008/06/13)

Urea substituted imidazoquinolines

-

, (2008/06/13)

Imidazoquinoline and tetrahydroimidazoquinoline compounds that contain urea, thiourea, acylurea, or sulfonylurea functionality at the 1-position are useful as immune response modifiers. The compounds and compositions of the invention can induce the biosynthesis of various cytokines and are useful in the treatment of a variety of conditions including viral diseases and neoplastic diseases.

Sulfonamide and sulfamide substituted imidazoquinolines

-

, (2008/06/13)

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