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Benzonitrile, 4-(phenylmethoxy)-3-[4-(phenylmethoxy)butoxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

858673-95-7

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858673-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 858673-95-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,8,6,7 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 858673-95:
(8*8)+(7*5)+(6*8)+(5*6)+(4*7)+(3*3)+(2*9)+(1*5)=237
237 % 10 = 7
So 858673-95-7 is a valid CAS Registry Number.

858673-95-7Relevant academic research and scientific papers

Purinenucleoside derivative modified in 8-position and medical use thereof

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Page/Page column 28, (2010/11/28)

The present invention provides an 8-modified purinenucleoside derivative which is useful for diseases associated with an abnormality of plasma uric acid level. An 8-modified purinenucleoside derivative represented by the following formula (I), a prodrug thereof or a pharmaceutically acceptable salt thereof, or a hydrate or solvate thereof, is useful for the prevention or treatment of gout, hyperuricemia, urinary lithiasis, hyperuricemic nephropathy or the like. In the formula, n is 1 or 2; RA is a hydrogen atom or a hydroxyl group; R1 is a hydrogen atom, a hydroxyl group, a thiol group, an amino group or a chlorine atom; ring J represents an optionally substituted 2-naphthyl group, or a group represented by the following general formula (II) wherein Y represents a single bond or a connecting group; ring Z represents an optionally substituted aryl group or heteroaryl group or the like; and R2 to R4, P1 and Q represents a halogen atom, a cyano group or the like.

BENZIMIDAZOLE DERIVATIVES AND MEDICAL USES THEREOF

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Page/Page column 31, (2008/06/13)

The present invention providesbenzimidazole derivatives represented by the following formula (I) or pharmaceutically acceptable salts thereof, or prodrugs thereof, which exert an inhibitory activity on sodium-dependent nucleoside transporter 2 and are useful for a disease associated with an abnormality of plasma uric acid level. The compounds of the present invention are useful for the prevention or treatment of gout, hyperuricemia, urinary lithiasis, hyperuricemic nephropathy or the like. In the formula, n is 1 or 2; R1 and R2 are H, a halogen atom, cyano group, optionally substituted alkyl group, optionally substituted aryl group or the like; R3 is H, a halogen atom, optionally substituted alkyl group or the like; R9 and R5 are H, a halogen atom, OH or the like; and R6 and RX are H or OH: RY is F or OH.

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