Cas 1094375-97-9,tert-butyl [(1E)-({(4R)-5-[(4-tert-butoxybenzyl)amino]-4-[(diphenylacetyl)amino]-5-oxopentyl}amino)({4-[4-(15-{1-[4-({(1E)-({(4R)-5-[(tert-butoxybenzyl)amino]-4-[(diphenylacetyl)amino]-5-oxopentyl}amino)[(tert-butoxycarbonyl)amino]methylene}amino)-4-oxobutyl]-1H-1,2,3-triazol-4-yl}-2,5,8,11,14-pentaoxapentadec-1-yl)-1H-1,2,3-triazol-1-yl]butanoyl}amino)methylene]carbamate

1094375-97-9

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Product Name: tert-butyl [(1E)-({(4R)-5-[(4-tert-butoxybenzyl)amino]-4-[(diphenylacetyl)amino]-5-oxopentyl}amino)({4-[4-(15-{1-[4-({(1E)-({(4R)-5-[(tert-butoxybenzyl)amino]-4-[(diphenylacetyl)amino]-5-oxopentyl}amino)[(tert-butoxycarbonyl)amino]methylene}amino)-4-oxobutyl]-1H-1,2,3-triazol-4-yl}-2,5,8,11,14-pentaoxapentadec-1-yl)-1H-1,2,3-triazol-1-yl]butanoyl}amino)methylene]carbamate
Synonyms: tert-butyl [(1E)-({(4R)-5-[(4-tert-butoxybenzyl)amino]-4-[(diphenylacetyl)amino]-5-oxopentyl}amino)({4-[4-(15-{1-[4-({(1E)-({(4R)-5-[(tert-butoxybenzyl)amino]-4-[(diphenylacetyl)amino]-5-oxopentyl}amino)[(tert-butoxycarbonyl)amino]methylene}amino)-4-oxobutyl]-1H-1,2,3-triazol-4-yl}-2,5,8,11,14-pentaoxapentadec-1-yl)-1H-1,2,3-triazol-1-yl]butanoyl}amino)methylene]carbamate
CAS NO:1094375-97-9
Molecular Formula:
Molecular Weight: 1752.13
EINECS: N/A
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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 [(1E)-({(4R)-5-[(4-tert-butoxybenzyl)amino]-4-[(diphenylacetyl)amino]-5-oxopentyl}amino)({4-[4-(15-{1-[4-({(1E)-({(4R)-5-[(tert-butoxybenzyl)amino]-4-[(diphenylacetyl)amino]-5-oxopentyl}amino)[(tert-butoxycarbonyl)amino]methylene}amino)-4-oxobutyl]-1H-1,2,3-triazol-4-yl}-2,5,8,11,14-pentaoxapentadec-1-yl)-1H-1,2,3-triazol-1-yl]butanoyl}amino)methylene]carbamate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl [(1E)-({(4R)-5-[(4-tert-butoxybenzyl)amino]-4-[(diphenylacetyl)amino]-5-oxopentyl}amino)({4-[4-(15-{1-[4-({(1E)-({(4R)-5-[(tert-butoxybenzyl)amino]-4-[(diphenylacetyl)amino]-5-oxopentyl}amino)[(tert-butoxycarbonyl)amino]methylene}amino)-4-oxobutyl]-1H-1,2,3-triazol-4-yl}-2,5,8,11,14-pentaoxapentadec-1-yl)-1H-1,2,3-triazol-1-yl]butanoyl}amino)methylene]carbamate(1094375-97-9)
EPA Substance Registry System: tert-butyl [(1E)-({(4R)-5-[(4-tert-butoxybenzyl)amino]-4-[(diphenylacetyl)amino]-5-oxopentyl}amino)({4-[4-(15-{1-[4-({(1E)-({(4R)-5-[(tert-butoxybenzyl)amino]-4-[(diphenylacetyl)amino]-5-oxopentyl}amino)[(tert-butoxycarbonyl)amino]methylene}amino)-4-oxobutyl]-1H-1,2,3-triazol-4-yl}-2,5,8,11,14-pentaoxapentadec-1-yl)-1H-1,2,3-triazol-1-yl]butanoyl}amino)methylene]carbamate(1094375-97-9)

Safety Data

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1094375-97-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1094375-97-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,4,3,7 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1094375-97:
(9*1)+(8*0)+(7*9)+(6*4)+(5*3)+(4*7)+(3*5)+(2*9)+(1*7)=179
179 % 10 = 9
So 1094375-97-9 is a valid CAS Registry Number.

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1094375-97-9Relevant academic research and scientific papers

Modular synthesis of non-peptidic bivalent NPY Y1 receptor antagonists

Weiss, Stefan,Keller, Max,Bernhardt, Guenther,Buschauer, Armin,Koenig, Burkhard

experimental part, p. 9858 - 9866 (2009/04/06)

According to a 'bivalent ligand approach' to increase the affinity of the potent argininamide-type NPY Y1 receptor antagonist BIBP-3226, dimeric ligands were synthesized in which two molecules of the parent compound were linked by different spacers via NG-acylation at the guanidino groups. A synthetic route for the preparation of the title compounds was developed, which includes a copper(I)-catalyzed azide alkyne cycloaddition as the key step. Three bivalent analogues of BIBP-3226 were prepared showing nanomolar antagonistic activity and binding affinity to the NPY Y1 receptor (calcium assay on HEL cells, radioligand binding assay on SK-N-MC cells), but these ligands were not superior to the parent compound and there was no correlation with the length or the chemical nature of the spacer. A trivalent BIBP-3226 derivate showed, surprisingly, no affinity to the NPY Y1 receptor at all.

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