Cas 897031-58-2,benzylthio β-D-xylopyranosyl-(1->4)-tetra[β-D-xylopyranosyl-(1->4)]-β-D-xylopyranoside

897031-58-2

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Basic information

Product Name: benzylthio β-D-xylopyranosyl-(1->4)-tetra[β-D-xylopyranosyl-(1->4)]-β-D-xylopyranoside
Synonyms: benzylthio β-D-xylopyranosyl-(1->4)-tetra[β-D-xylopyranosyl-(1->4)]-β-D-xylopyranoside
CAS NO:897031-58-2
Molecular Formula:
Molecular Weight: 916.903
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: benzylthio β-D-xylopyranosyl-(1->4)-tetra[β-D-xylopyranosyl-(1->4)]-β-D-xylopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: benzylthio β-D-xylopyranosyl-(1->4)-tetra[β-D-xylopyranosyl-(1->4)]-β-D-xylopyranoside(897031-58-2)
EPA Substance Registry System: benzylthio β-D-xylopyranosyl-(1->4)-tetra[β-D-xylopyranosyl-(1->4)]-β-D-xylopyranoside(897031-58-2)

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: 897031-58-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 897031-58-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,7,0,3 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 897031-58:
(8*8)+(7*9)+(6*7)+(5*0)+(4*3)+(3*1)+(2*5)+(1*8)=202
202 % 10 = 2
So 897031-58-2 is a valid CAS Registry Number.

897031-58-2Upstream product

897031-58-2Downstream Products

897031-58-2Relevant academic research and scientific papers

Glycosynthase-based synthesis of xylo-oligosaccharides using an engineered retaining xylanase from Cellulomonas fimi

Kim, Young-Wan,Fox, David T.,Hekmat, Omid,Kantner, Terrence,McIntosh, Lawrence P.,Warren, R. Antony J.,Withers, Stephen G.

, p. 2025 - 2032 (2008/09/18)

Glycosynthases are synthetic enzymes derived from retaining glycosidases in which the catalytic nucleophile has been replaced. The mutation allows irreversible glycosylation of sugar acceptors using glycosyl fluoride donors to afford oligosaccharides with

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