Cas 1067651-14-2,(2R,6S,7aR)-tert-butyl 2-(6-(tert-butyldiphenylsilanyloxy)-2-oxo-6,7-dihydro-2H-benzofuran-7a-yl)piperidine-1-carboxylate

1067651-14-2

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Basic information

Product Name: (2R,6S,7aR)-tert-butyl 2-(6-(tert-butyldiphenylsilanyloxy)-2-oxo-6,7-dihydro-2H-benzofuran-7a-yl)piperidine-1-carboxylate
Synonyms: (2R,6S,7aR)-tert-butyl 2-(6-(tert-butyldiphenylsilanyloxy)-2-oxo-6,7-dihydro-2H-benzofuran-7a-yl)piperidine-1-carboxylate
CAS NO:1067651-14-2
Molecular Formula:
Molecular Weight: 573.805
EINECS: N/A
Product Categories: N/A
Mol File: 1067651-14-2.mol
Article Data: 1

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: (2R,6S,7aR)-tert-butyl 2-(6-(tert-butyldiphenylsilanyloxy)-2-oxo-6,7-dihydro-2H-benzofuran-7a-yl)piperidine-1-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: (2R,6S,7aR)-tert-butyl 2-(6-(tert-butyldiphenylsilanyloxy)-2-oxo-6,7-dihydro-2H-benzofuran-7a-yl)piperidine-1-carboxylate(1067651-14-2)
EPA Substance Registry System: (2R,6S,7aR)-tert-butyl 2-(6-(tert-butyldiphenylsilanyloxy)-2-oxo-6,7-dihydro-2H-benzofuran-7a-yl)piperidine-1-carboxylate(1067651-14-2)

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: 1067651-14-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1067651-14-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,7,6,5 and 1 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1067651-14:
(9*1)+(8*0)+(7*6)+(6*7)+(5*6)+(4*5)+(3*1)+(2*1)+(1*4)=152
152 % 10 = 2
So 1067651-14-2 is a valid CAS Registry Number.

1067651-14-2Upstream product

86953-81-3 tert-butyl 2-hydroxypiperidine-1-carboxylate

1067651-14-2Downstream Products

1067651-14-2Relevant articles and documents

Diastereoselective synthesis of allosecurinine and viroallosecurinine from menisdaurilide

Bardaji, Gisela G.,Canto, Mariona,Alibes, Ramon,Bayon, Pau,Busque, Felix,De March, Pedro,Figueredo, Marta,Font, Josep

experimental part, p. 7657 - 7662 (2009/04/11)

(Chemical Equation Presented) A new and versatile synthetic route to Securinega alkaloids is reported. The first synthesis of allosecurinine has been accomplished in seven steps and 40% yield, starting from (+)-menisdaurilide, using a vinylogous Mannich reaction as the key transformation. Similarly, viroallosecurinine has been synthesized from (-)-menisdaurilide.

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