Cas 1310357-43-7,(((4R,5R)-4-((1S,3R)-5-(benzyloxy)-1-methoxy-3-methylpentyl)-2,2-dimethyl-1,3-dioxan-5-yl)oxy)triethylsilane

1310357-43-7

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Basic information

Product Name: (((4R,5R)-4-((1S,3R)-5-(benzyloxy)-1-methoxy-3-methylpentyl)-2,2-dimethyl-1,3-dioxan-5-yl)oxy)triethylsilane
Synonyms: (((4R,5R)-4-((1S,3R)-5-(benzyloxy)-1-methoxy-3-methylpentyl)-2,2-dimethyl-1,3-dioxan-5-yl)oxy)triethylsilane
CAS NO:1310357-43-7
Molecular Formula:
Molecular Weight: 466.734
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: (((4R,5R)-4-((1S,3R)-5-(benzyloxy)-1-methoxy-3-methylpentyl)-2,2-dimethyl-1,3-dioxan-5-yl)oxy)triethylsilane(CAS DataBase Reference)
NIST Chemistry Reference: (((4R,5R)-4-((1S,3R)-5-(benzyloxy)-1-methoxy-3-methylpentyl)-2,2-dimethyl-1,3-dioxan-5-yl)oxy)triethylsilane(1310357-43-7)
EPA Substance Registry System: (((4R,5R)-4-((1S,3R)-5-(benzyloxy)-1-methoxy-3-methylpentyl)-2,2-dimethyl-1,3-dioxan-5-yl)oxy)triethylsilane(1310357-43-7)

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: 1310357-43-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1310357-43-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,0,3,5 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1310357-43:
(9*1)+(8*3)+(7*1)+(6*0)+(5*3)+(4*5)+(3*7)+(2*4)+(1*3)=107
107 % 10 = 7
So 1310357-43-7 is a valid CAS Registry Number.

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1310357-43-7Relevant academic research and scientific papers

Synthesis of key fragments of leiodelide A

Chellat, Mathieu F.,Proust, Nicolas,Lauer, Matthew G.,Stambuli, James P.

, p. 3246 - 3249 (2011)

The synthesis of all key fragments of the marine macrolide leiodelide A is described. The polyoxygenated northern subunit is derived from d-xylose, while the southern subunit is rapidly assembled via an aldol reaction and Horner-Wadsworth-Emmons olefination. This highly convergent approach will allow for rapid modification and assembly of several isomers of leiodelide A, which may be necessary considering the assignment of leiodelide B has been previously shown to be incorrect.

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