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N,N'-((1Z,3Z)-1,4-bis(4-methoxyphenyl)buta-1,3-diene-2,3-diyl)diformamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

112271-44-0

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112271-44-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112271-44-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,2,7 and 1 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 112271-44:
(8*1)+(7*1)+(6*2)+(5*2)+(4*7)+(3*1)+(2*4)+(1*4)=80
80 % 10 = 0
So 112271-44-0 is a valid CAS Registry Number.

112271-44-0Downstream Products

112271-44-0Relevant academic research and scientific papers

FORMYLATED XANTHOCILLIN ANALOGUES AS NEUROPROTECTIVE AGENTS

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, (2015/02/18)

Formylated xanthocillin analogs can be used in the treatment of neurodegenerative diseases. The analogs can be prepared synthetically, and at least some of the analogs can be obtained from a microorganism strain of the Penicillium chrysogenum species.

FORMYLATED XANTHOCILLIN ANALOGUES AS NEUROPROTECTANTS

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Page/Page column 64, (2015/01/18)

The present invention relates to formylated xanthocillin analogues for use in the treatment of neurodegenerative diseases, to some of said analogues, as well as to methods for obtaining them and pharmaceutical composition comprising them. The invention al

ALPHA-SUBSTITUTED VINYLTIN COMPOUND

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Page/Page column 22, (2009/02/11)

To provide α-substituted vinyltin useful for the search for function-developing substances such as pharmaceuticals/agrichemicals and functional materials and for the construction of a compound library. An α-substituted vinyltin compound represented by the

The first stereoselective total synthesis of antiviral antibiotic, xanthocillin X dimethylether and its stereoisomer

Tatsuta, Kuniaki,Yamaguchi, Takahiro

, p. 5017 - 5020 (2007/10/03)

Xanthocillin X dimethylether (1) has been stereoselectively synthesized from the propiolic acid 6 through an oxidative rearrangement of the stannyl vinyl amide 27 to give the vinyl isocyanate 30 and a homocoupling of the stannyl N-formylenamine 31.

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