Cas 1309477-56-2,tert-butyl 4-(benzyloxymethoxy)-3-((dimethoxyphosphoryloxy)methyl)butanoate

1309477-56-2

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Basic information

Product Name: tert-butyl 4-(benzyloxymethoxy)-3-((dimethoxyphosphoryloxy)methyl)butanoate
Synonyms: tert-butyl 4-(benzyloxymethoxy)-3-((dimethoxyphosphoryloxy)methyl)butanoate
CAS NO:1309477-56-2
Molecular Formula:
Molecular Weight: 418.424
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: tert-butyl 4-(benzyloxymethoxy)-3-((dimethoxyphosphoryloxy)methyl)butanoate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl 4-(benzyloxymethoxy)-3-((dimethoxyphosphoryloxy)methyl)butanoate(1309477-56-2)
EPA Substance Registry System: tert-butyl 4-(benzyloxymethoxy)-3-((dimethoxyphosphoryloxy)methyl)butanoate(1309477-56-2)

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: 1309477-56-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1309477-56-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,9,4,7 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1309477-56:
(9*1)+(8*3)+(7*0)+(6*9)+(5*4)+(4*7)+(3*7)+(2*5)+(1*6)=172
172 % 10 = 2
So 1309477-56-2 is a valid CAS Registry Number.

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1309477-56-2Relevant academic research and scientific papers

The first total synthesis of (±)-cyclophostin and (±)-cyclipostin P: Inhibitors of the serine hydrolases acetyl cholinesterase and hormone sensitive lipase

Malla, Raj K.,Bandyopadhyay, Saibal,Spilling, Christopher D.,Dutta, Supratik,Dupureur, Cynthia M.

, p. 3094 - 3097 (2011)

Cyclophostin, a structurally unique and potent naturally occurring acetyl cholinesterase (AChE) inhibitor, and its unnatural diastereomer were prepared in 6 steps and 15% overall yield from hydroxymethyl butyrolactone. The unnatural diastereomer of cyclop

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