Cas 866408-90-4,(4R,5R)-2-[(Z)-3-(Dimethyl-phenyl-silanyl)-allyl]-[1,3,2]dioxaborolane-4,5-dicarboxylic acid diisopropyl ester

866408-90-4

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Basic information

Product Name: (4R,5R)-2-[(Z)-3-(Dimethyl-phenyl-silanyl)-allyl]-[1,3,2]dioxaborolane-4,5-dicarboxylic acid diisopropyl ester
Synonyms:
CAS NO:866408-90-4
Molecular Formula:
Molecular Weight: 418.37
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)-2-[(Z)-3-(Dimethyl-phenyl-silanyl)-allyl]-[1,3,2]dioxaborolane-4,5-dicarboxylic acid diisopropyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (4R,5R)-2-[(Z)-3-(Dimethyl-phenyl-silanyl)-allyl]-[1,3,2]dioxaborolane-4,5-dicarboxylic acid diisopropyl ester(866408-90-4)
EPA Substance Registry System: (4R,5R)-2-[(Z)-3-(Dimethyl-phenyl-silanyl)-allyl]-[1,3,2]dioxaborolane-4,5-dicarboxylic acid diisopropyl ester(866408-90-4)

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: 866408-90-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 866408-90-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,4,0 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 866408-90:
(8*8)+(7*6)+(6*6)+(5*4)+(4*0)+(3*8)+(2*9)+(1*0)=204
204 % 10 = 4
So 866408-90-4 is a valid CAS Registry Number.

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866408-90-4Relevant academic research and scientific papers

Synthesis of (+)-bullatacin via the highly diastereoselective [3+2] annulation reaction of a racemic aldehyde and a nonracemic allylsilane

Tinsley, Jennifer M.,Mertz, Eric,Chong, Pek Y.,Rarig, Robert-Andre F.,Roush, William R.

, p. 4245 - 4248 (2005)

(Chemical Equation Presented) A total synthesis of (+)-bullatacin has been accomplished via a diastereoselective [3+2] annulation reaction of the highly enantiomerically enriched allylsilane 3 and racemic aldehyde 4, which provides the key bis-tetrahydrof

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