Cas 866090-31-5,2-cyanoethyl (2',3'-di-O-benzoyl-uridin-5'-yl) vinylphosphonate

866090-31-5

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Basic information

Product Name: 2-cyanoethyl (2',3'-di-O-benzoyl-uridin-5'-yl) vinylphosphonate
Synonyms:
CAS NO:866090-31-5
Molecular Formula:
Molecular Weight: 595.502
EINECS: N/A
Product Categories: N/A
Mol File: 866090-31-5.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: 2-cyanoethyl (2',3'-di-O-benzoyl-uridin-5'-yl) vinylphosphonate(CAS DataBase Reference)
NIST Chemistry Reference: 2-cyanoethyl (2',3'-di-O-benzoyl-uridin-5'-yl) vinylphosphonate(866090-31-5)
EPA Substance Registry System: 2-cyanoethyl (2',3'-di-O-benzoyl-uridin-5'-yl) vinylphosphonate(866090-31-5)

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: 866090-31-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 866090-31-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,0,9 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 866090-31:
(8*8)+(7*6)+(6*6)+(5*0)+(4*9)+(3*0)+(2*3)+(1*1)=185
185 % 10 = 5
So 866090-31-5 is a valid CAS Registry Number.

866090-31-5Upstream product

50408-20-3 2',3'-di-O-benzoyluridine

866090-31-5Downstream Products

866090-31-5Relevant articles and documents

Selective cross-metathesis of C-allyl-glycosides

Timmer, Mattie S. M.,Chumillas, Marta Vinciano,Donker-Koopman, Wilma E.,Aerts, Johannes M. F. G.,Van Der Marel, Gijsbert A.,Overkleeft, Herman S.,Van Boom, Jacques H.

, p. 335 - 351 (2005)

The efficient and selective cross-metathesis (CM) of both the α- and β-anomers of C-allyl-glucose and N-acetyl-C-allyl-glucosamine with electron-deficient olefins is reported. The applicability of our CM approach in the synthesis of glycoside-conjugates i

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