Cas 1160616-08-9,tert-butyl (1S,3R,5S,6S,7S)-3-(tert-butyl)-7-chloro-6-benzyloxy-7-(2-benzyloxy)ethyl-2-oxa-4-azabicyclo[3.2.0]heptane-4-carboxylate

1160616-08-9

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Basic information

Product Name: tert-butyl (1S,3R,5S,6S,7S)-3-(tert-butyl)-7-chloro-6-benzyloxy-7-(2-benzyloxy)ethyl-2-oxa-4-azabicyclo[3.2.0]heptane-4-carboxylate
Synonyms: tert-butyl (1S,3R,5S,6S,7S)-3-(tert-butyl)-7-chloro-6-benzyloxy-7-(2-benzyloxy)ethyl-2-oxa-4-azabicyclo[3.2.0]heptane-4-carboxylate
CAS NO:1160616-08-9
Molecular Formula:
Molecular Weight: 530.104
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: tert-butyl (1S,3R,5S,6S,7S)-3-(tert-butyl)-7-chloro-6-benzyloxy-7-(2-benzyloxy)ethyl-2-oxa-4-azabicyclo[3.2.0]heptane-4-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (1S,3R,5S,6S,7S)-3-(tert-butyl)-7-chloro-6-benzyloxy-7-(2-benzyloxy)ethyl-2-oxa-4-azabicyclo[3.2.0]heptane-4-carboxylate(1160616-08-9)
EPA Substance Registry System: tert-butyl (1S,3R,5S,6S,7S)-3-(tert-butyl)-7-chloro-6-benzyloxy-7-(2-benzyloxy)ethyl-2-oxa-4-azabicyclo[3.2.0]heptane-4-carboxylate(1160616-08-9)

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: 1160616-08-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1160616-08-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,0,6,1 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1160616-08:
(9*1)+(8*1)+(7*6)+(6*0)+(5*6)+(4*1)+(3*6)+(2*0)+(1*8)=119
119 % 10 = 9
So 1160616-08-9 is a valid CAS Registry Number.

1160616-08-9Upstream product

1160616-08-9Downstream Products

1160616-09-0 (1R,2S,3R,4S)-4-amino-3-(benzyloxy)-2-[2-(benzyloxy)ethyl]-2-chlorocyclobutanol

1160616-08-9Relevant academic research and scientific papers

Synthesis of enantiopure α-chlorocyclobutanones and cyclobutanols as scaffolds for the diverted synthesis of serine protease inhibitors

Yang, Gaoqiang,Ghosez, Leon

experimental part, p. 1738 - 1748 (2009/08/17)

Synthetic paths towards highly functionalized α-chlorocyclobutanone scaffolds susceptible to lead to serine proteases inhibitors were explored. The syntheses started from bicyclic α-chlorocyclobutanones 3, which are readily available from Seebach's oxazol

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