Cas 883236-93-9,3-{(R)-1-[2-(2-Amino-acetylamino)-phenyl]-8-ethyl-5,6,7,8-tetrahydro-indolizin-8-yl}-propionic acid

883236-93-9

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Basic information

Product Name: 3-{(R)-1-[2-(2-Amino-acetylamino)-phenyl]-8-ethyl-5,6,7,8-tetrahydro-indolizin-8-yl}-propionic acid
Synonyms: 3-{(R)-1-[2-(2-Amino-acetylamino)-phenyl]-8-ethyl-5,6,7,8-tetrahydro-indolizin-8-yl}-propionic acid
CAS NO:883236-93-9
Molecular Formula:
Molecular Weight: 369.464
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: 3-{(R)-1-[2-(2-Amino-acetylamino)-phenyl]-8-ethyl-5,6,7,8-tetrahydro-indolizin-8-yl}-propionic acid(CAS DataBase Reference)
NIST Chemistry Reference: 3-{(R)-1-[2-(2-Amino-acetylamino)-phenyl]-8-ethyl-5,6,7,8-tetrahydro-indolizin-8-yl}-propionic acid(883236-93-9)
EPA Substance Registry System: 3-{(R)-1-[2-(2-Amino-acetylamino)-phenyl]-8-ethyl-5,6,7,8-tetrahydro-indolizin-8-yl}-propionic acid(883236-93-9)

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: 883236-93-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 883236-93-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,3,2,3 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 883236-93:
(8*8)+(7*8)+(6*3)+(5*2)+(4*3)+(3*6)+(2*9)+(1*3)=199
199 % 10 = 9
So 883236-93-9 is a valid CAS Registry Number.

883236-93-9Upstream product

883236-93-9Downstream Products

883236-93-9Relevant academic research and scientific papers

Synthesis and biological evaluation of B-ring analogues of (-)-rhazinilam

Decor, Anne,Monse, Barbara,Martin, Marie-Therese,Chiaroni, Angele,Thoret, Sylviane,Guenard, Daniel,Gueritte, Francoise,Baudoin, Olivier

, p. 2314 - 2332 (2007/10/03)

Three macrocyclic analogues of rhazinilam 1 having a 11- or 12-membered B-ring with an endocyclic carbamate group or an amino-acid residue were synthesized from the natural product. These analogues 3 and 4 displayed a very low activity on tubulin. Thirty

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