Cas 905307-70-2,[3(2R,3S),4R]-3-[2,3-bis-(tert-butyldimethylsilyloxy)-4-methyl-1-oxopentyl]-4-benzyl-1,3-oxazolidin-2-one

905307-70-2

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Basic information

Product Name: [3(2R,3S),4R]-3-[2,3-bis-(tert-butyldimethylsilyloxy)-4-methyl-1-oxopentyl]-4-benzyl-1,3-oxazolidin-2-one
Synonyms: [3(2R,3S),4R]-3-[2,3-bis-(tert-butyldimethylsilyloxy)-4-methyl-1-oxopentyl]-4-benzyl-1,3-oxazolidin-2-one
CAS NO:905307-70-2
Molecular Formula:
Molecular Weight: 535.872
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: [3(2R,3S),4R]-3-[2,3-bis-(tert-butyldimethylsilyloxy)-4-methyl-1-oxopentyl]-4-benzyl-1,3-oxazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: [3(2R,3S),4R]-3-[2,3-bis-(tert-butyldimethylsilyloxy)-4-methyl-1-oxopentyl]-4-benzyl-1,3-oxazolidin-2-one(905307-70-2)
EPA Substance Registry System: [3(2R,3S),4R]-3-[2,3-bis-(tert-butyldimethylsilyloxy)-4-methyl-1-oxopentyl]-4-benzyl-1,3-oxazolidin-2-one(905307-70-2)

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: 905307-70-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 905307-70-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,5,3,0 and 7 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 905307-70:
(8*9)+(7*0)+(6*5)+(5*3)+(4*0)+(3*7)+(2*7)+(1*0)=152
152 % 10 = 2
So 905307-70-2 is a valid CAS Registry Number.

905307-70-2Upstream product

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905307-70-2Relevant academic research and scientific papers

Asymmetric induction in methyl ketone aldol additions to α-alkoxy and α,β-bisalkoxy aldehydes: A model for acyclic stereocontrol

Evans, David A.,Cee, Victor J.,Siska, Sarah J.

, p. 9433 - 9441 (2007/10/03)

A systematic study of methyl ketone aldol additions under nonchelating conditions with α-alkoxy and α,β-bisalkoxy aldehydes is described. Additions to aldehydes containing a single α-alkoxy stereocenter generally provide the product diastereomers in accor

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