Cas 1027343-76-5,ethyl (2S,1'R,2'R,3'R,5'R)-2-[(2'-tert-butoxycarbonylamino)-6',6'-dimethylbicyclo[3.3.1]heptane-3'-carbonyl]amino-3-phenylpropionate

1027343-76-5

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Basic information

Product Name: ethyl (2S,1'R,2'R,3'R,5'R)-2-[(2'-tert-butoxycarbonylamino)-6',6'-dimethylbicyclo[3.3.1]heptane-3'-carbonyl]amino-3-phenylpropionate
Synonyms:
CAS NO:1027343-76-5
Molecular Formula:
Molecular Weight: 458.598
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: ethyl (2S,1'R,2'R,3'R,5'R)-2-[(2'-tert-butoxycarbonylamino)-6',6'-dimethylbicyclo[3.3.1]heptane-3'-carbonyl]amino-3-phenylpropionate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl (2S,1'R,2'R,3'R,5'R)-2-[(2'-tert-butoxycarbonylamino)-6',6'-dimethylbicyclo[3.3.1]heptane-3'-carbonyl]amino-3-phenylpropionate(1027343-76-5)
EPA Substance Registry System: ethyl (2S,1'R,2'R,3'R,5'R)-2-[(2'-tert-butoxycarbonylamino)-6',6'-dimethylbicyclo[3.3.1]heptane-3'-carbonyl]amino-3-phenylpropionate(1027343-76-5)

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: 1027343-76-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1027343-76-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,7,3,4 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1027343-76:
(9*1)+(8*0)+(7*2)+(6*7)+(5*3)+(4*4)+(3*3)+(2*7)+(1*6)=125
125 % 10 = 5
So 1027343-76-5 is a valid CAS Registry Number.

1027343-76-5Upstream product

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1027343-76-5Relevant academic research and scientific papers

Regio- and stereoselective synthesis of constrained enantiomeric β-amino acid derivatives

Szakonyi, Zsolt,Martinek, Tamas A.,Sillanpaeae, Reijo,Fueloep, Ferenc

, p. 2296 - 2303 (2008)

Chlorosulfonyl isocyanate addition to (-)- and (+)-apopinene furnished monoterpene-fused β-lactams in highly regio- and stereospecific reactions. β-Lactams 5 and 13 exhibited reactivities similar to those of the cycloalkane-fused analogs and were easily c

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