Cas 1450880-22-4,Z-dimethyl-4’-(3-benzoyl-2,4-dioxo-pyrimidin-1-yl)-3’-(acetyloxymethyl)-but-2’-enylphosphonate

1450880-22-4

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Basic information

Product Name: Z-dimethyl-4’-(3-benzoyl-2,4-dioxo-pyrimidin-1-yl)-3’-(acetyloxymethyl)-but-2’-enylphosphonate
Synonyms: Z-dimethyl-4’-(3-benzoyl-2,4-dioxo-pyrimidin-1-yl)-3’-(acetyloxymethyl)-but-2’-enylphosphonate
CAS NO:1450880-22-4
Molecular Formula:
Molecular Weight: 450.385
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: Z-dimethyl-4’-(3-benzoyl-2,4-dioxo-pyrimidin-1-yl)-3’-(acetyloxymethyl)-but-2’-enylphosphonate(CAS DataBase Reference)
NIST Chemistry Reference: Z-dimethyl-4’-(3-benzoyl-2,4-dioxo-pyrimidin-1-yl)-3’-(acetyloxymethyl)-but-2’-enylphosphonate(1450880-22-4)
EPA Substance Registry System: Z-dimethyl-4’-(3-benzoyl-2,4-dioxo-pyrimidin-1-yl)-3’-(acetyloxymethyl)-but-2’-enylphosphonate(1450880-22-4)

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: 1450880-22-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1450880-22-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,0,8,8 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1450880-22:
(9*1)+(8*4)+(7*5)+(6*0)+(5*8)+(4*8)+(3*0)+(2*2)+(1*2)=154
154 % 10 = 4
So 1450880-22-4 is a valid CAS Registry Number.

1450880-22-4Upstream product

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1450880-22-4Relevant academic research and scientific papers

The preparation of trisubstituted alkenyl nucleoside phosphonates under ultrasound-assisted olefin cross-metathesis

Sari, Ozkan,Hamada, Manabu,Roy, Vincent,Nolan, Steven P.,Agrofoglio, Luigi A.

, p. 4390 - 4393 (2013/09/24)

Intermolecular ultrasound-assisted olefin cross-metathesis is reported. This approach allows an easy access to challenging trisubstituted alkenyl nucleoside phosphonates. Regioselective chemoenzymatic deacetylation and Mitsunobu coupling are also describe

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