Cas 500795-46-0,Silane, [(1E,4R,5S)-5-(methoxymethoxy)-4-[(2S,4S,5S)-2-(4-methoxyphenyl)-5- methyl-5-(1-propynyl)-1,3-dioxolan-4-yl]-2-methyl-1-decenyl]trimethyl-

500795-46-0

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Basic information

Product Name: Silane, [(1E,4R,5S)-5-(methoxymethoxy)-4-[(2S,4S,5S)-2-(4-methoxyphenyl)-5- methyl-5-(1-propynyl)-1,3-dioxolan-4-yl]-2-methyl-1-decenyl]trimethyl-
Synonyms:
CAS NO:500795-46-0
Molecular Formula: C30H48O5Si
Molecular Weight: 516.794
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: Silane, [(1E,4R,5S)-5-(methoxymethoxy)-4-[(2S,4S,5S)-2-(4-methoxyphenyl)-5- methyl-5-(1-propynyl)-1,3-dioxolan-4-yl]-2-methyl-1-decenyl]trimethyl-(CAS DataBase Reference)
NIST Chemistry Reference: Silane, [(1E,4R,5S)-5-(methoxymethoxy)-4-[(2S,4S,5S)-2-(4-methoxyphenyl)-5- methyl-5-(1-propynyl)-1,3-dioxolan-4-yl]-2-methyl-1-decenyl]trimethyl-(500795-46-0)
EPA Substance Registry System: Silane, [(1E,4R,5S)-5-(methoxymethoxy)-4-[(2S,4S,5S)-2-(4-methoxyphenyl)-5- methyl-5-(1-propynyl)-1,3-dioxolan-4-yl]-2-methyl-1-decenyl]trimethyl-(500795-46-0)

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: 500795-46-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 500795-46-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,0,7,9 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 500795-46:
(8*5)+(7*0)+(6*0)+(5*7)+(4*9)+(3*5)+(2*4)+(1*6)=140
140 % 10 = 0
So 500795-46-0 is a valid CAS Registry Number.

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500795-46-0Relevant academic research and scientific papers

Total synthesis of formamicin

Durham, Timothy B.,Blanchard, Nicolas,Savall, Brad M.,Powell, Noel A.,Roush, William R.

, p. 9307 - 9317 (2007/10/03)

The enantioselective total synthesis of the cytotoxic plecomacrolide natural product formamicin (1) is described. Key aspects of this synthesis include the efficient transacetalation reactions of MOM ethers 28 and 38 to form the seven-membered formyl acet

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