Cas 160409-00-7,(3R,4S)-3-(Benzyloxy)-1-(tert-butoxycarbonyl)-4-<(S)-2,2-dimethyl-1,3-dioxolan-4-yl>azetidin-2-one

160409-00-7

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Basic information

Product Name: (3R,4S)-3-(Benzyloxy)-1-(tert-butoxycarbonyl)-4-<(S)-2,2-dimethyl-1,3-dioxolan-4-yl>azetidin-2-one
Synonyms: (3R,4S)-3-(Benzyloxy)-1-(tert-butoxycarbonyl)-4-<(S)-2,2-dimethyl-1,3-dioxolan-4-yl>azetidin-2-one
CAS NO:160409-00-7
Molecular Formula:
Molecular Weight: 377.437
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: (3R,4S)-3-(Benzyloxy)-1-(tert-butoxycarbonyl)-4-<(S)-2,2-dimethyl-1,3-dioxolan-4-yl>azetidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (3R,4S)-3-(Benzyloxy)-1-(tert-butoxycarbonyl)-4-<(S)-2,2-dimethyl-1,3-dioxolan-4-yl>azetidin-2-one(160409-00-7)
EPA Substance Registry System: (3R,4S)-3-(Benzyloxy)-1-(tert-butoxycarbonyl)-4-<(S)-2,2-dimethyl-1,3-dioxolan-4-yl>azetidin-2-one(160409-00-7)

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: 160409-00-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 160409-00-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,4,0 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 160409-00:
(8*1)+(7*6)+(6*0)+(5*4)+(4*0)+(3*9)+(2*0)+(1*0)=97
97 % 10 = 7
So 160409-00-7 is a valid CAS Registry Number.

160409-00-7Upstream product

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160409-00-7Relevant academic research and scientific papers

Concise General Synthesis of α,γ-Disubstituted β-Amino Ketones from β-Lactams

Palomo, Claudio,Aizpurua, Jesus M.,Garcia, Jesus M.,Iturubu, Miren,Odriozola, Jose M.

, p. 5184 - 5188 (1994)

α,γ-Disubstituted β-amino ketones were obtained by ring opening of 3,4-disubstituted N-Boc-β-lactams, promoted by Grignard and organocuprate reagents.

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