Cas 540490-41-3,(1R,5R)-3-Phenyl-1-trimethylsilanyl-3-aza-bicyclo[3.2.1]octane-2,4-dione

540490-41-3

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Basic information

Product Name: (1R,5R)-3-Phenyl-1-trimethylsilanyl-3-aza-bicyclo[3.2.1]octane-2,4-dione
Synonyms: (1R,5R)-3-Phenyl-1-trimethylsilanyl-3-aza-bicyclo[3.2.1]octane-2,4-dione
CAS NO:540490-41-3
Molecular Formula:
Molecular Weight: 287.434
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: (1R,5R)-3-Phenyl-1-trimethylsilanyl-3-aza-bicyclo[3.2.1]octane-2,4-dione(CAS DataBase Reference)
NIST Chemistry Reference: (1R,5R)-3-Phenyl-1-trimethylsilanyl-3-aza-bicyclo[3.2.1]octane-2,4-dione(540490-41-3)
EPA Substance Registry System: (1R,5R)-3-Phenyl-1-trimethylsilanyl-3-aza-bicyclo[3.2.1]octane-2,4-dione(540490-41-3)

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: 540490-41-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 540490-41-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,0,4,9 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 540490-41:
(8*5)+(7*4)+(6*0)+(5*4)+(4*9)+(3*0)+(2*4)+(1*1)=133
133 % 10 = 3
So 540490-41-3 is a valid CAS Registry Number.

540490-41-3Upstream product

75-77-4 chloro-trimethyl-silane

540490-41-3Downstream Products

540490-50-4 (1R,4R,5R)-4-Hydroxy-3-phenyl-1-trimethylsilanyl-3-aza-bicyclo[3.2.1]octan-2-one

540490-41-3Relevant academic research and scientific papers

Bridgehead enolates: Substitution and asymmetric desymmetrization of small bridged carbonyl compounds by lithium amide bases

Giblin, Gerard M. P.,Kirk, Douglas T.,Mitchell, Lee,Simpkins, Nigel S.

, p. 1673 - 1675 (2003)

(Matrix presented) Contrary to expectations, a number of bridged carbonyl compounds undergo facile bridgehead metalation with lithium amide bases. Diketone, lactone, lactam, and imide functions are all demonstrated to participate in this type of "bridgehe

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