Cas 104841-33-0,b-D-Mannopyranoside,O-(1R)-4-O-(2,4-dihydroxy-6-methylbenzoyl)-2,3-O-methylene-D-xylopyranosylidene-(1®3-4)-a-L-lyxopyranosyl O-3-amino-2,3,6-trideoxy-3-C-methyl-4-O-methyl-a-L-arabino-hexopyranosyl-(1®3)-O-2,6-dideoxy-4-O-(3,5-dichloro-4-hydroxy-2-methoxy-6-methylbenzoyl)-b-D-arabino-hexopyranosyl-(1®4)-O-2,6-dideoxy-D-arabino-hexopyranosylidene-(1®3-4)-O-6-deoxy-3-C-methyl-b-D-mannopyranosyl-(1®3)-O-6-deoxy-4-O-methyl-b-D-galactopyranosyl-(1®4)-2,6-di-O-methyl- (9CI)

104841-33-0

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Product Name: b-D-Mannopyranoside,O-(1R)-4-O-(2,4-dihydroxy-6-methylbenzoyl)-2,3-O-methylene-D-xylopyranosylidene-(1®3-4)-a-L-lyxopyranosyl O-3-amino-2,3,6-trideoxy-3-C-methyl-4-O-methyl-a-L-arabino-hexopyranosyl-(1®3)-O-2,6-dideoxy-4-O-(3,5-dichloro-4-hydroxy-2-methoxy-6-methylbenzoyl)-b-D-arabino-hexopyranosyl-(1®4)-O-2,6-dideoxy-D-arabino-hexopyranosylidene-(1®3-4)-O-6-deoxy-3-C-methyl-b-D-mannopyranosyl-(1®3)-O-6-deoxy-4-O-methyl-b-D-galactopyranosyl-(1®4)-2,6-di-O-methyl- (9CI)
Synonyms: Flambamycin,12-O-(3-amino-2,3,6-trideoxy-3-C-methyl-4-O-methyl-a-L-arabino-hexopyranosyl)-56-deacetyl-57-demethyl-45-O-de(2-methyl-1-oxopropyl)-,56-(2,4-dihydroxy-6-methylbenzoate); 2,4'-Spirobi[4H-1,3-dioxolo[4,5-c]pyran],flambamycin deriv.; Spiro[4H-1,3-dioxolo[4,5-c]pyran-2,2'-[2H]pyran],flambamycin deriv.; Antibiotic 13-384-5; SCH 27900
CAS NO:104841-33-0
Molecular Formula: C70H99 Cl2 N O36
Molecular Weight: 1601.45
EINECS: N/A
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Chemical Properties

Melting Point: N/A
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Density: N/A
Refractive Index: N/A
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CAS DataBase Reference: b-D-Mannopyranoside,O-(1R)-4-O-(2,4-dihydroxy-6-methylbenzoyl)-2,3-O-methylene-D-xylopyranosylidene-(1®3-4)-a-L-lyxopyranosyl O-3-amino-2,3,6-trideoxy-3-C-methyl-4-O-methyl-a-L-arabino-hexopyranosyl-(1®3)-O-2,6-dideoxy-4-O-(3,5-dichloro-4-hydroxy-2-methoxy-6-methylbenzoyl)-b-D-arabino-hexopyranosyl-(1®4)-O-2,6-dideoxy-D-arabino-hexopyranosylidene-(1®3-4)-O-6-deoxy-3-C-methyl-b-D-mannopyranosyl-(1®3)-O-6-deoxy-4-O-methyl-b-D-galactopyranosyl-(1®4)-2,6-di-O-methyl- (9CI)(CAS DataBase Reference)
NIST Chemistry Reference: b-D-Mannopyranoside,O-(1R)-4-O-(2,4-dihydroxy-6-methylbenzoyl)-2,3-O-methylene-D-xylopyranosylidene-(1®3-4)-a-L-lyxopyranosyl O-3-amino-2,3,6-trideoxy-3-C-methyl-4-O-methyl-a-L-arabino-hexopyranosyl-(1®3)-O-2,6-dideoxy-4-O-(3,5-dichloro-4-hydroxy-2-methoxy-6-methylbenzoyl)-b-D-arabino-hexopyranosyl-(1®4)-O-2,6-dideoxy-D-arabino-hexopyranosylidene-(1®3-4)-O-6-deoxy-3-C-methyl-b-D-mannopyranosyl-(1®3)-O-6-deoxy-4-O-methyl-b-D-galactopyranosyl-(1®4)-2,6-di-O-methyl- (9CI)(104841-33-0)
EPA Substance Registry System: b-D-Mannopyranoside,O-(1R)-4-O-(2,4-dihydroxy-6-methylbenzoyl)-2,3-O-methylene-D-xylopyranosylidene-(1®3-4)-a-L-lyxopyranosyl O-3-amino-2,3,6-trideoxy-3-C-methyl-4-O-methyl-a-L-arabino-hexopyranosyl-(1®3)-O-2,6-dideoxy-4-O-(3,5-dichloro-4-hydroxy-2-methoxy-6-methylbenzoyl)-b-D-arabino-hexopyranosyl-(1®4)-O-2,6-dideoxy-D-arabino-hexopyranosylidene-(1®3-4)-O-6-deoxy-3-C-methyl-b-D-mannopyranosyl-(1®3)-O-6-deoxy-4-O-methyl-b-D-galactopyranosyl-(1®4)-2,6-di-O-methyl- (9CI)(104841-33-0)

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Hazardous Substances Data: 104841-33-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 104841-33-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,8,4 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104841-33:
(8*1)+(7*0)+(6*4)+(5*8)+(4*4)+(3*1)+(2*3)+(1*3)=100
100 % 10 = 0
So 104841-33-0 is a valid CAS Registry Number.

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104841-33-0Relevant academic research and scientific papers

Chemical modifications and structure activity studies of ziracin and related everninomicin antibiotics

Ganguly, Ashit K.,McCormick, Jinping L.,Saksena, Anil K.,Das, Pradip R.,Chan, Tze-Ming

, p. 1209 - 1214 (2007/10/03)

Chemical modifications of eveminomicin antibiotics, particularly ziracin (1), were carried out to study the SAILs as well as the chemical properties of this class of compounds. Use of allyl ether group for protection and selective deprotection of phenolic groups provided access to a variety of novel analogs of the title compounds, some of which exhibited the same high in vitro potency as the parent compounds.

The structure of new oligosaccharide antibiotics, 13-384 components 1 and 5

Ganguly,Pramanik,Chan,Sarre,Liu,Morton,Girijavallabhan

, p. 83 - 88 (2007/10/02)

Structures of 13-384 antibiotics have been deduced based on chemical degradation and spectroscopic evidence.

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