Cas 436099-13-7,2,3-di-O-acetyl-4-azido-6-O-benzoyl-4-deoxy-β-D-glucopyranosyl-(1->4)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl fluoride

436099-13-7

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Basic information

Product Name: 2,3-di-O-acetyl-4-azido-6-O-benzoyl-4-deoxy-β-D-glucopyranosyl-(1->4)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl fluoride
Synonyms: 2,3-di-O-acetyl-4-azido-6-O-benzoyl-4-deoxy-β-D-glucopyranosyl-(1->4)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl fluoride
CAS NO:436099-13-7
Molecular Formula:
Molecular Weight: 683.598
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: 2,3-di-O-acetyl-4-azido-6-O-benzoyl-4-deoxy-β-D-glucopyranosyl-(1->4)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl fluoride(CAS DataBase Reference)
NIST Chemistry Reference: 2,3-di-O-acetyl-4-azido-6-O-benzoyl-4-deoxy-β-D-glucopyranosyl-(1->4)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl fluoride(436099-13-7)
EPA Substance Registry System: 2,3-di-O-acetyl-4-azido-6-O-benzoyl-4-deoxy-β-D-glucopyranosyl-(1->4)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl fluoride(436099-13-7)

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: 436099-13-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 436099-13-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,6,0,9 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 436099-13:
(8*4)+(7*3)+(6*6)+(5*0)+(4*9)+(3*9)+(2*1)+(1*3)=157
157 % 10 = 7
So 436099-13-7 is a valid CAS Registry Number.

436099-13-7Upstream product

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436099-13-7Relevant academic research and scientific papers

Chemoenzymatic synthesis of a bifunctionalized cellohexaoside as a specific substrate for the sensitive assay of cellulase by fluorescence quenching

Boyer, Viviane,Fort, Sebastien,Frandsen, Torben P.,Schuelein, Martin,Cottaz, Sylvain,Driguez, Hugues

, p. 1389 - 1394 (2007/10/03)

A new bifunctionalized cellohexaose derivative was synthesized as a specific substrate for continuous assay of cellulases by resonance energy transfer. This cellohexaoside has a naphthalene moiety (EDANS) as a fluorescent energy donor at the reducing end

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