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6835-26-3

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6835-26-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6835-26-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,3 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6835-26:
(6*6)+(5*8)+(4*3)+(3*5)+(2*2)+(1*6)=113
113 % 10 = 3
So 6835-26-3 is a valid CAS Registry Number.

6835-26-3Upstream product

6835-26-3Relevant articles and documents

Magnetic and spectral properties of adducts of copper(II) chlorobenzoates with substituted piperazines

Manhas,Kalia,Sardana,Lumba

, p. 1226 - 1232 (2008/03/27)

Adducts of Cu(OOCR)2 (where R = 2-, 3- or 4-ClC 6H4) with saturated substituted piperazines of the type Cu(OOCR)2(L-L)n [where n = 0.5 or 1 and L-L = 1-methylpiperazine (1-MePipz), 1,4-dimethylpiperazine (l,4-Me2Pipz). 2,6-dimethylpiperazine (2,6-Me2Pipz) and 1-phenylpiperazine (1-PhPipz)] have been prepared and characterized by elemental analysis, infrared, electronic reflectance, electron paramagnetic resonance spectral and magnetic moment studies. Three complexes which have room temperature magnetic moment values lower than the spin only values and have room temperature electron paramagnetic resonance spectra corresponding to S = 1, rather than S = 1/2, have been further subjected to magnetic susceptibility and electron paramagnetic resonance spectral measurements at different temperatures to evaluate spin-exchange parameter (-2J = 282-313 cm-1). Based upon the above studies, axially symmetric binuclear structure for complexes of the type Cu(OOCR)2(L-L), polymeric structure containing binuclear units for the Cu(OOCR)2(L-L)0.5 complexes and axially symmetric polymeric square pyramidal or trans-pseudo octahedral structure for complexes of the type Cu(OOCR)2(2,6-Me2Pipz) (R = 2-, 3- and 4-ClC6H4), have been proposed.

Antiallergic cyclic sulphur compounds

-

, (2008/06/13)

Certain tricyclic thioxanthone-10,10-dioxide compounds each of which is substituted in the 1-,2-,3- or 4-position by a carboxyl or (5-tetrazolyl) group and each of which is optionally substituted in the 5-,6-,7- or 8-position by a second carboxyl or (5-tetrazolyl) group or a substituent selected from cyano, halogen, nitro, alkyl, alkoxy, acyl, amino, acylamino, thioalkyl, alkylsulphinyl and alkylsulphonyl, as well as salts, and optionally substituted esters and amides of the carboxyl substituted compounds and alkyl derivatives of the tetrazolyl substituted compounds, are useful for the relief or prophylaxis of allergic conditions.

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