Cas 404579-63-1,diallyl [phenyl 2-acetamido-3-O-benzoyl-2,4-dideoxy-β-L-threo-hex-4-enopyranoside-6-yl]-phosphonate

404579-63-1

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Basic information

Product Name: diallyl [phenyl 2-acetamido-3-O-benzoyl-2,4-dideoxy-β-L-threo-hex-4-enopyranoside-6-yl]-phosphonate
Synonyms: diallyl [phenyl 2-acetamido-3-O-benzoyl-2,4-dideoxy-β-L-threo-hex-4-enopyranoside-6-yl]-phosphonate
CAS NO:404579-63-1
Molecular Formula:
Molecular Weight: 543.51
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: diallyl [phenyl 2-acetamido-3-O-benzoyl-2,4-dideoxy-β-L-threo-hex-4-enopyranoside-6-yl]-phosphonate(CAS DataBase Reference)
NIST Chemistry Reference: diallyl [phenyl 2-acetamido-3-O-benzoyl-2,4-dideoxy-β-L-threo-hex-4-enopyranoside-6-yl]-phosphonate(404579-63-1)
EPA Substance Registry System: diallyl [phenyl 2-acetamido-3-O-benzoyl-2,4-dideoxy-β-L-threo-hex-4-enopyranoside-6-yl]-phosphonate(404579-63-1)

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: 404579-63-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 404579-63-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,4,5,7 and 9 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 404579-63:
(8*4)+(7*0)+(6*4)+(5*5)+(4*7)+(3*9)+(2*6)+(1*3)=151
151 % 10 = 1
So 404579-63-1 is a valid CAS Registry Number.

404579-63-1Upstream product

404579-63-1Downstream Products

404579-63-1Relevant academic research and scientific papers

Efficient sialyltransferase inhibitors based on glycosides of N-acetylglucosamine

Schwoerer, Ralf,Schmidt, Richard R.

, p. 1632 - 1637 (2007/10/03)

D-Glucosamine was transformed into phenyl and 2-benzoyloxyethyl N-acetylglucosamine β-glycosides 6a and 6b, respectively. Transformation of 6a,b into 6-O-unprotected N-acetylglucosamine derivatives 9a,b permitted the generation of an aldehyde group in the

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