Cas 35520-98-0,3,4,-di-O-acetyl-β-D-fructofuranosyl 2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside

35520-98-0

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Basic information

Product Name: 3,4,-di-O-acetyl-β-D-fructofuranosyl 2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside
Synonyms: 3,4,-di-O-acetyl-β-D-fructofuranosyl 2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside
CAS NO:35520-98-0
Molecular Formula:
Molecular Weight: 594.524
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: 3,4,-di-O-acetyl-β-D-fructofuranosyl 2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: 3,4,-di-O-acetyl-β-D-fructofuranosyl 2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside(35520-98-0)
EPA Substance Registry System: 3,4,-di-O-acetyl-β-D-fructofuranosyl 2,3,4,6-tetra-O-acetyl-α-D-glucopyranoside(35520-98-0)

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: 35520-98-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 35520-98-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,5,2 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 35520-98:
(7*3)+(6*5)+(5*5)+(4*2)+(3*0)+(2*9)+(1*8)=110
110 % 10 = 0
So 35520-98-0 is a valid CAS Registry Number.

35520-98-0Upstream product

126-14-7 sucrose octaacetate

35520-98-0Downstream Products

35520-98-0Relevant academic research and scientific papers

Regioselective Enzymatic Deacetylation of Sucrose Octaacetate in Organic Solvents.

Palmer, David C.,Terradas, Fernand

, p. 1673 - 1676 (2007/10/02)

The first examples of deacetylation of sucrose octaacetate using proteases and lipases in organic solvents are reported.The regiochemistry of the product sucrose hepta-, hexa- and pentaacetates was established by perdeuteroacetylation and 1H-NMR.Preparation of key intermediates in the commerical synthesis of the high intensity sweetener, sucralose was achieved.

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