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MeO-Oxalyl-L-Thr-D-allo-Thr-D-Tyr-NH2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1027554-48-8

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1027554-48-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1027554-48-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,5,5 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1027554-48:
(9*1)+(8*0)+(7*2)+(6*7)+(5*5)+(4*5)+(3*4)+(2*4)+(1*8)=138
138 % 10 = 8
So 1027554-48-8 is a valid CAS Registry Number.

1027554-48-8Upstream product

1027554-48-8Downstream Products

1027554-48-8Relevant academic research and scientific papers

Structure elucidation of Sch 20562, a glucosidic cyclic dehydropeptide lactone: The major component of W-10 antifungal antibiotic

Afonso, Adriano,Hon, Frank,Brambilla, Ray

, p. 383 - 397 (2007/10/03)

A novel bacterium designated as Aeromonas sp. W-10 produces the antibiotic W-10 complex which comprises of two major and several minor components. The two major components from this complex, Sch 20562 (1) and Sch 20561 (1a), are of biological interest in view of their potent antifungal activity. The chemical degradation studies utilized for the assignment of structure 1 for Sch 20562 are described here. Some of the noteworthy diversity of structural features in this glucosidic cyclic dehydrononapeptide lactone 1 are: an N-terminal (D)-β-hydroxymyristyl unit, three D-amino acid units, two (E)-α-aminocrotonyl units, and an O-α-D-glucosyl-N-methyl-L-allo-threonine unit. The structure determination of 1 utilized the selective cleavage of the dehydropeptide units by ozonolysis to form fragments that were sequenced by mass spectrometry. The stereochemistry of the amino acid units were assigned by isolation of the free amino acids from the hydrolysates of the fragments. The stereochemistry of the α-aminocrotonyl units and the glucosidic linkage were assigned by nmr spectroscopy and molecular rotation data.

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