Cas 220126-19-2,(1'S,1''S,2S,5'R,8'S)-2-[2'-(1''-Phenylethyl)-3',7'-dioxa-2'-azabicyclo[3.3.0]octan-8'-yl]-3-oxahex-5-en-1-ol

220126-19-2

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Basic information

Product Name: (1'S,1''S,2S,5'R,8'S)-2-[2'-(1''-Phenylethyl)-3',7'-dioxa-2'-azabicyclo[3.3.0]octan-8'-yl]-3-oxahex-5-en-1-ol
Synonyms:
CAS NO:220126-19-2
Molecular Formula:
Molecular Weight: 319.401
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'S,1''S,2S,5'R,8'S)-2-[2'-(1''-Phenylethyl)-3',7'-dioxa-2'-azabicyclo[3.3.0]octan-8'-yl]-3-oxahex-5-en-1-ol(CAS DataBase Reference)
NIST Chemistry Reference: (1'S,1''S,2S,5'R,8'S)-2-[2'-(1''-Phenylethyl)-3',7'-dioxa-2'-azabicyclo[3.3.0]octan-8'-yl]-3-oxahex-5-en-1-ol(220126-19-2)
EPA Substance Registry System: (1'S,1''S,2S,5'R,8'S)-2-[2'-(1''-Phenylethyl)-3',7'-dioxa-2'-azabicyclo[3.3.0]octan-8'-yl]-3-oxahex-5-en-1-ol(220126-19-2)

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: 220126-19-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 220126-19-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,1,2 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 220126-19:
(8*2)+(7*2)+(6*0)+(5*1)+(4*2)+(3*6)+(2*1)+(1*9)=72
72 % 10 = 2
So 220126-19-2 is a valid CAS Registry Number.

220126-19-2Upstream product

65973-54-8 (2R,3R)-2,3-Bis-allyloxy-succinic acid diethyl ester

220126-19-2Downstream Products

220126-19-2Relevant academic research and scientific papers

Cycloadducts from highly functionalized nitrones and oximes as ligands in the enantioselective addition of diethylzinc to benzaldehyde

Baskaran, Subramanian,Aurich, Hans Guenter,Biesemeier, Frank,Harms, Klaus

, p. 3717 - 3724 (2007/10/03)

Highly diastereoselective intramolecular cycloaddition of nitrones 5-7 and 16, as well as oximes 11-13 that are easily accessible from diethyl (R,R)-tartrate, affords bicyclic compounds 8-10 and 17. The tetracyclic compound 14 is formed as the main produc

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