Cas 128848-29-3,benzyl 3-O-<4-O-(4-O-methyl-2,3,6-tridesoxy-α-L-erythro-hex-2-enopyranosyl)-3-O-benzoyl-2,6-dideoxy-2-iodo-α-L-altropyranosyl>-4-O-benzyl-2,6-dideoxy-α-L-ribo-hexopyranoside

128848-29-3

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Basic information

Product Name: benzyl 3-O-<4-O-(4-O-methyl-2,3,6-tridesoxy-α-L-erythro-hex-2-enopyranosyl)-3-O-benzoyl-2,6-dideoxy-2-iodo-α-L-altropyranosyl>-4-O-benzyl-2,6-dideoxy-α-L-ribo-hexopyranoside
Synonyms:
CAS NO:128848-29-3
Molecular Formula:
Molecular Weight: 814.712
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: benzyl 3-O-<4-O-(4-O-methyl-2,3,6-tridesoxy-α-L-erythro-hex-2-enopyranosyl)-3-O-benzoyl-2,6-dideoxy-2-iodo-α-L-altropyranosyl>-4-O-benzyl-2,6-dideoxy-α-L-ribo-hexopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: benzyl 3-O-<4-O-(4-O-methyl-2,3,6-tridesoxy-α-L-erythro-hex-2-enopyranosyl)-3-O-benzoyl-2,6-dideoxy-2-iodo-α-L-altropyranosyl>-4-O-benzyl-2,6-dideoxy-α-L-ribo-hexopyranoside(128848-29-3)
EPA Substance Registry System: benzyl 3-O-<4-O-(4-O-methyl-2,3,6-tridesoxy-α-L-erythro-hex-2-enopyranosyl)-3-O-benzoyl-2,6-dideoxy-2-iodo-α-L-altropyranosyl>-4-O-benzyl-2,6-dideoxy-α-L-ribo-hexopyranoside(128848-29-3)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 128848-29-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 128848-29-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,8,4 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 128848-29:
(8*1)+(7*2)+(6*8)+(5*8)+(4*4)+(3*8)+(2*2)+(1*9)=163
163 % 10 = 3
So 128848-29-3 is a valid CAS Registry Number.

128848-29-3Upstream product

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128848-29-3Relevant academic research and scientific papers

Syntheses of kijanimicin oligosaccharides

Thiem, Joachim,Koepper, Sabine

, p. 113 - 138 (2007/10/02)

Various di- and trisaccharide precursors of the kijanimicin tetrasaccharide were prepared by the N-iodosuccinimide glycosylation procedure employing regioselectively blocked L-digitoxosides and L-digitoxals. Assumed 13-neighboring group participations wer

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