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IMidafenacin IMpurity (1-(3-Cyano-3,3-Diphenylpropyl)-2-Methyl-1H-IMidazoliuM Phosphate) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

562091-56-9

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562091-56-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 562091-56-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,2,0,9 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 562091-56:
(8*5)+(7*6)+(6*2)+(5*0)+(4*9)+(3*1)+(2*5)+(1*6)=149
149 % 10 = 9
So 562091-56-9 is a valid CAS Registry Number.

562091-56-9Downstream Products

562091-56-9Relevant academic research and scientific papers

2,4-(1H, 3H)-quinazolinedione derivative and synthesis method and use thereof

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, (2016/12/22)

The present invention discloses a 2,4-(1H,3H)-quinazolinedione derivative and a synthesis method and use thereof, belongs to the technical field of medicines, and relates to the 2,4-(1H, 3H)-quinazolinedione derivative shown as general formula(I), wherein R1 is O(CH2)n-1H, n=1-10; or NH(CH2)n-2H, n=2-10; or NH(CH2)n-3(CH3)2, n=3-10; or N(CH2)n-4, n=6-10; or NH(CH2)n-5 C6H4-L, n=5-10; R2 is H; or X-O(CH2)n-1H, n=1-10; or X-NH(CH2)n-2(CH3)2, n=2-10; X is m-CH2C6H4CO; L is independently selected from the group consisting of H, F, Cl, Br, I, CN, NO2, CF3, OCF3, SCF3, OH, SH, NH2, COOR, R, OR, SR, NHR, NRR, OCOR, SCOR and NHCOR, wherein R is C1-6 straight chain alkyl, branched alkyl or alicyclic alkyl or phenyl. Structures and the synthesis method and in-vitro acetylcholin esterase inhibition activity of the compounds are disclosed, and the compounds can be further developed as drugs for treating Alzheimer's disease.

METHOD FOR PRODUCING 4-(2-METHYL-1-IMIDAZOLYL)-2,2-PHENYLBUTANE AMIDE

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, (2016/12/22)

PROBLEM TO BE SOLVED: To provide a method for industrially producing 4-(2-methyl-1-imidazolyl)-2,2-diphenylbutane amide (imidafenacin), which is a selective muscarine receptor antagonist, in a high yield and purity. SOLUTION: Imidafenacin is produced by once isolating methane sulfonate or p-toluensulfonate of 4-(2-methyl-1-imidazolyl)-2,2-diphenylbutyronitrile, purifying it, and thereafter hydrolyzing it in a lower alcohol in the presence of an alkali metal oxide without neutralizing. COPYRIGHT: (C)2015,JPOandINPIT

PROCESS FOR PRODUCING MUSCARINE RECEPTOR ANTAGONIST AND INTERMEDIATE THEREFOR

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Page/Page column 4, (2008/06/13)

The industrial production of 4-(2-methyl-1-imidazolyl)-2,2-diphenylbutanamide, a urinary incontinence remedy, necessitates elimination of problems concerning the use of a synthetic adsorbent, e.g., HP-20, the efficiency of operation with the same, purification efficiency, etc. An acid salt, e.g., hydrochloride or phosphate, of 4-(2-methyl-1-imidazolyl)-2,2- diphenylbutanamide or a hydrate of any of these salts is used as an intermediate. This intermediate is neutralized and then purified. Thus, high-purity 4-(2-methyl -1-imidazolyl)-2,2-diphenylbutanamide is easily obtained in satisfactory yield. The industrial-scale production process has been thus established.

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