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1(3),2,4(6),5,6(4)-penta-O-acetyl-sn-myoinositol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35519-39-2

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35519-39-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35519-39-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,5,1 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 35519-39:
(7*3)+(6*5)+(5*5)+(4*1)+(3*9)+(2*3)+(1*9)=122
122 % 10 = 2
So 35519-39-2 is a valid CAS Registry Number.

35519-39-2Relevant academic research and scientific papers

Flexible stereo- and regioselective synthesis of myo-inositol phosphates (Part 2): Via nonsymmetrical conduritol B derivatives

Podeschwa, Michael A. L.,Plettenburg, Oliver,Altenbach, Hans-Josef

, p. 3116 - 3127 (2007/10/03)

A practical route is described for the preparation of myo-inositol phosphates. Optically pure compounds can be prepared, in both forms, from p-benzoquinone by enzymatic resolution of a diacetoxyconduritol key intermediate. Monosubstituted inositol derivat

INVESTIGATIONS IN THE REGION OF ASYMMETRICALLY SUBSTITUTED MYO-INOSITOL DERIVATIVES XXXIV. SYNTHESIS OF DIASTEREOMERIC ACETATES OF β-D-GLUCOSYL-MYO-INOSITOL AND CHIRAL MYO-INOSITOL PENTAACETATES

Sibrikov, Yu. I.,Stepanov, A. E.,Shvets, V. I.

, p. 899 - 904 (2007/10/02)

The glucosylation of racemic tetra- and pentaacetyl-myo-inositols by D-glucose tert-butylorthoacetate leads to a mixture of diastereomeric acetate derivatives of β-D-glucosyl-myo-inositol.Chiral pentaacetyl-myo-inositols were obtained from the synthesized

INVESTIGATIONS IN ASYMMETRICALLY SUBSTITUTED MYOINOSITOL DERIVATIVES. XXXII. SEPARATION OF RACEMIC 1(3),4(6),5,6(4)-TETRA-O-ACETYL-sn-MYOINOSITOL AND 1(3),2,4(6),5,6(4)-PENTA-O-ACETYL-sn-MYOINOSITOL THROUGH THE DIASTEREOMERIC ORTHO ESTERS WITH D-MANNOSE

Sibrikov, Yu. I.,Stepanov, A. E.,Shvets, V. I.

, p. 1089 - 1094 (2007/10/02)

Racemic 1(3),4(6),5,6(4)-tetra-O-acetyl-sn-myoinositol and 1(3),2,4(6),5,6(4)-penta-O-acetyl-sn-myoinositol were resolved into the optical antipodes by the formation and separation of the diastereomeric ortho esters with D-mannose.Acid hydrolysis of the s

INVESTIGATIONS IN THE FIELD OF ASYMMETRICALLY SUBSTITUTED MYOINOSITOL DERIVATIVES. XXX. REACTION OF 2,3-DIHYDROPYRAN WITH TETRASUBSTITUTED DERIVATIVES OF MYOINOSITOL

Stepanov, A. E.,Sibrikov, Yu. I.,Shvets, V. I.

, p. 1946 - 1950 (2007/10/02)

In the reaction of 2,3-dihydropyran with 1(3),4(6),5,6(4)-tetra-O-benzyl- and 1(3),4(6),5,6(4)-tetra-O-acetyl-sn-myoinositols the corresponding mono- and ditetrahydropyranyl ethers are formed.

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