Cas 1415686-95-1,(-)-1-[(1′,2′-dideoxy-3′,4′;5′,6′-di-O-isopropylene-1′-methoxycarbonylmethylene)-D-2′-glucosyl]-4β-[(1α,2α)-epoxy-1-methyl-2-phenylethyl]-3β-methoxy-2-azetidinone

1415686-95-1

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Product Name: (-)-1-[(1′,2′-dideoxy-3′,4′;5′,6′-di-O-isopropylene-1′-methoxycarbonylmethylene)-D-2′-glucosyl]-4β-[(1α,2α)-epoxy-1-methyl-2-phenylethyl]-3β-methoxy-2-azetidinone
Synonyms: (-)-1-[(1′,2′-dideoxy-3′,4′;5′,6′-di-O-isopropylene-1′-methoxycarbonylmethylene)-D-2′-glucosyl]-4β-[(1α,2α)-epoxy-1-methyl-2-phenylethyl]-3β-methoxy-2-azetidinone
CAS NO:1415686-95-1
Molecular Formula:
Molecular Weight: 531.603
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: (-)-1-[(1′,2′-dideoxy-3′,4′;5′,6′-di-O-isopropylene-1′-methoxycarbonylmethylene)-D-2′-glucosyl]-4β-[(1α,2α)-epoxy-1-methyl-2-phenylethyl]-3β-methoxy-2-azetidinone(CAS DataBase Reference)
NIST Chemistry Reference: (-)-1-[(1′,2′-dideoxy-3′,4′;5′,6′-di-O-isopropylene-1′-methoxycarbonylmethylene)-D-2′-glucosyl]-4β-[(1α,2α)-epoxy-1-methyl-2-phenylethyl]-3β-methoxy-2-azetidinone(1415686-95-1)
EPA Substance Registry System: (-)-1-[(1′,2′-dideoxy-3′,4′;5′,6′-di-O-isopropylene-1′-methoxycarbonylmethylene)-D-2′-glucosyl]-4β-[(1α,2α)-epoxy-1-methyl-2-phenylethyl]-3β-methoxy-2-azetidinone(1415686-95-1)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1415686-95-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1415686-95-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,6,8 and 6 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1415686-95:
(9*1)+(8*4)+(7*1)+(6*5)+(5*6)+(4*8)+(3*6)+(2*9)+(1*5)=181
181 % 10 = 1
So 1415686-95-1 is a valid CAS Registry Number.

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1415686-95-1Relevant academic research and scientific papers

Synthesis of polycyclic β-lactams. Evolution of tertiary radicals generated by Cp2TiCl from 1,5- and 1,6-epoxynitriles

Monleón, Laura M.,Grande, Manuel,Anaya, Josefa

, p. 10794 - 10805 (2012)

Radical cyclisation induced by Cp2TiCl of several 1,5- and 1,6-epoxynitriles derived from β-lactams gave 3-oxo-4-methyl-4- hydroxymethylcarbapenams or 4-oxo-5-methylbenzocarbacephems. Apart from these polycyclic β-lactams, the generated alkyl tertiary radicals also evolved to enamides through β-fragmentation and reduction and the tertiary homobenzyl radicals gave a 3,4-trans-6-hydroxymonolactam by hydrogen transfer.

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