Cas 1448711-05-4,methyl 5-acetamido-4-phenoxybutyrylamido-3,4,5-trideoxy-D-glycero-α-D-galacto-non-2-ulopyranosidonic acid sodium salt

1448711-05-4

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Basic information

Product Name: methyl 5-acetamido-4-phenoxybutyrylamido-3,4,5-trideoxy-D-glycero-α-D-galacto-non-2-ulopyranosidonic acid sodium salt
Synonyms: methyl 5-acetamido-4-phenoxybutyrylamido-3,4,5-trideoxy-D-glycero-α-D-galacto-non-2-ulopyranosidonic acid sodium salt
CAS NO:1448711-05-4
Molecular Formula:
Molecular Weight: 506.485
EINECS: N/A
Product Categories: N/A
Mol File: 1448711-05-4.mol
Article Data: 1

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: methyl 5-acetamido-4-phenoxybutyrylamido-3,4,5-trideoxy-D-glycero-α-D-galacto-non-2-ulopyranosidonic acid sodium salt(CAS DataBase Reference)
NIST Chemistry Reference: methyl 5-acetamido-4-phenoxybutyrylamido-3,4,5-trideoxy-D-glycero-α-D-galacto-non-2-ulopyranosidonic acid sodium salt(1448711-05-4)
EPA Substance Registry System: methyl 5-acetamido-4-phenoxybutyrylamido-3,4,5-trideoxy-D-glycero-α-D-galacto-non-2-ulopyranosidonic acid sodium salt(1448711-05-4)

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: 1448711-05-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1448711-05-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,8,7,1 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1448711-05:
(9*1)+(8*4)+(7*4)+(6*8)+(5*7)+(4*1)+(3*1)+(2*0)+(1*5)=164
164 % 10 = 4
So 1448711-05-4 is a valid CAS Registry Number.

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1448711-05-4Relevant articles and documents

C-4 modified sialosides enhance binding to Siglec-2 (CD22): Towards potent Siglec inhibitors for immunoglycotherapy

Kelm, S?rge,Madge, Paul,Islam, Tasneem,Bennett, Ryan,Koliwer-Brandl, Hendrik,Waespy, Mario,Von Itzstein, Mark,Haselhorst, Thomas

, p. 3616 - 3620 (2013/05/21)

Two changes for the better: A novel class of sialic acid derivatives is prepared by modifying both the C-4 and C-9 positions of Neu5Aα2Me (see structure). This approach gives a lead compound that has sub-micromolar affinity for Siglec-2 and may provide a pathway for immunoglycotherapy strategies for autoimmune diseases and B cell derived non-Hodgkin's lymphoma. Copyright

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