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13035-68-2

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13035-68-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13035-68-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,3 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 13035-68:
(7*1)+(6*3)+(5*0)+(4*3)+(3*5)+(2*6)+(1*8)=72
72 % 10 = 2
So 13035-68-2 is a valid CAS Registry Number.

13035-68-2Relevant academic research and scientific papers

Tetrakisphosphates and Bispyrophosphates of myo-Inositol Derivatives as Allosteric Effectors of Human Hemoglobin: Synthesis, Molecular Recognition, and Oxygen Release

Koumbis, Alexandros E.,Duarte, Carolina D.,Nicolau, Claude,Lehn, Jean-Marie

, p. 169 - 180 (2013/01/09)

Various 2,5- and 1,4-substituted and unsubstituted myo-inositol tetrakisphosphates and bispyrophosphates were prepared following a general synthetic pathway. All final compounds were tested for their capability to induce oxygen release from human hemoglob

Synthesis of 5-deoxy-5,5-difluoro-myo-inositol-1,2,6-tris(phosphate)

Ballereau, Stephanie,Spiess, Bernard,Schlewer, Gilbert

, p. 139 - 146 (2007/10/03)

5-deoxy-5,5-difluoro-mvo-inositol-1,2,6-tris(phosphate), a fluorinated analogue of α-trinositol, (D-myo-inositol-1,2,6-tris(phosphate)) was prepared from myo-inositol. After selective protection the remaining hydroxyl in position 5 was oxidized by a Swern

Total synthesis of (+)-polyoxin J starting from myo-inositol

Chida,Koizumi,Kitada,Yokoyama,Ogawa

, p. 111 - 113 (2007/10/02)

The total synthesis of the antifungal antibiotic, polyoxin J starting from myo-inositol is described; the two key components, were prepared from a pair of optically resolved myo-inositol derivatives , respectively, using a highly regioselective Baeyer-Vil

THE TOTAL SYNTHESIS OF myo-INOSITOL POLYPHOSPHATES

Vacca, Joseph P.,deSolms, S. Jane,Huff, Joel R.,Billington, David C.,Baker, Raymond,et al.

, p. 5679 - 5702 (2007/10/02)

Total synthesis of the individual enentiomers of myo-inositol 4-phosphate (15), myo-inositol 1,4-biphosphate (2) and myo-inositol 1,4,5-triphosphate (1), together with syntheses of racemic myo-inositol 1,3,4-triphosphate (4) and myo-inositol 2,4,5-triphos

Synthesis of Optically Active myo-Inositol 1,3,4-Triphosphate

Ozaki, Shoichiro,Kohno, Masayasu,Nakahira, Hiroyuki,Bunya, Motonobu,Watanabe, Yutaka

, p. 77 - 80 (2007/10/02)

Synthesis of optically active myo-inositol 1,3,4-triphosphate has been accomplished.Efficiency of a chiral HPLC column for optical resolution of myo-inositols is shown.

THE PREPARATION OF CYCLOHEXANEPENTOLS FROM INOSITOLS BY DEOXYGENATION

Angyal, Stephen J.,Odier, Leon

, p. 209 - 220 (2007/10/02)

Several cyclohexapenetols heva been synthesized from inositols by blocking all but one hydroxyl group, converting the free hydroxyl group into its S-methyl dithiocarbonate, and treating it with tributylstannane.Suitable blocking-groups are methyl, benzyl, and methylthiomethyl ethers, and acetals.One cyclohexanepentol was prepared by the reductive deamination of an aminodeoxyinositol.

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