Cas 223418-06-2,Dibenzyl-{(2E,4E)-(S)-1-[3-(tert-butyl-dimethyl-silanyloxy)-propyl]-5-phenyl-penta-2,4-dienyl}-amine

223418-06-2

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Basic information

Product Name: Dibenzyl-{(2E,4E)-(S)-1-[3-(tert-butyl-dimethyl-silanyloxy)-propyl]-5-phenyl-penta-2,4-dienyl}-amine
Synonyms: Dibenzyl-{(2E,4E)-(S)-1-[3-(tert-butyl-dimethyl-silanyloxy)-propyl]-5-phenyl-penta-2,4-dienyl}-amine
CAS NO:223418-06-2
Molecular Formula:
Molecular Weight: 511.823
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: Dibenzyl-{(2E,4E)-(S)-1-[3-(tert-butyl-dimethyl-silanyloxy)-propyl]-5-phenyl-penta-2,4-dienyl}-amine(CAS DataBase Reference)
NIST Chemistry Reference: Dibenzyl-{(2E,4E)-(S)-1-[3-(tert-butyl-dimethyl-silanyloxy)-propyl]-5-phenyl-penta-2,4-dienyl}-amine(223418-06-2)
EPA Substance Registry System: Dibenzyl-{(2E,4E)-(S)-1-[3-(tert-butyl-dimethyl-silanyloxy)-propyl]-5-phenyl-penta-2,4-dienyl}-amine(223418-06-2)

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: 223418-06-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 223418-06-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,3,4,1 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 223418-06:
(8*2)+(7*2)+(6*3)+(5*4)+(4*1)+(3*8)+(2*0)+(1*6)=102
102 % 10 = 2
So 223418-06-2 is a valid CAS Registry Number.

223418-06-2Upstream product

52378-69-5 diethyl (E)-cinnamylphosphonate

223418-06-2Downstream Products

223418-07-3 2,2,4,4-Tetramethyl-oxazolidine-3-carboxylic acid (5E,7E)-(S)-4-dibenzylamino-8-phenyl-octa-5,7-dienyl ester

223418-06-2Relevant academic research and scientific papers

(-)-Sparteine-mediated stereoselective intramolecular conjugate addition reactions of dienes and enynes

Oestreich,Hoppe

, p. 1881 - 1884 (1999)

Enantioenriched carbanionic pairs generated by the asymmetric deprotonation of carbamate esters with the chiral base s-butyllithium/(-)- sparteine undergo smoothly intramolecular conjugate addition reactions to dienes and enynes in high yields.

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