Cas 230627-29-9,(4-benzoyl-5-methyl-1-{pentanoyl-[2'-(1-trityl-1<i>H</i>-tetrazol-5-yl)-biphenyl-4-ylmethyl]-amino}-1<i>H</i>-pyrrol-2-yl)-acetic acid methyl ester

230627-29-9

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Basic information

Product Name: (4-benzoyl-5-methyl-1-{pentanoyl-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-amino}-1H-pyrrol-2-yl)-acetic acid methyl ester
Synonyms: (4-benzoyl-5-methyl-1-{pentanoyl-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-amino}-1H-pyrrol-2-yl)-acetic acid methyl ester
CAS NO:230627-29-9
Molecular Formula:
Molecular Weight: 833.002
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: (4-benzoyl-5-methyl-1-{pentanoyl-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-amino}-1H-pyrrol-2-yl)-acetic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (4-benzoyl-5-methyl-1-{pentanoyl-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-amino}-1H-pyrrol-2-yl)-acetic acid methyl ester(230627-29-9)
EPA Substance Registry System: (4-benzoyl-5-methyl-1-{pentanoyl-[2'-(1-trityl-1H-tetrazol-5-yl)-biphenyl-4-ylmethyl]-amino}-1H-pyrrol-2-yl)-acetic acid methyl ester(230627-29-9)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 230627-29-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 230627-29-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,0,6,2 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 230627-29:
(8*2)+(7*3)+(6*0)+(5*6)+(4*2)+(3*7)+(2*2)+(1*9)=109
109 % 10 = 9
So 230627-29-9 is a valid CAS Registry Number.

230627-29-9Upstream product

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230627-29-9Relevant academic research and scientific papers

Synthesis of biphenylyltetrazole derivatives of 1-aminopyrroles as angiotensin II antagonists

Attanasi, Orazio A.,Colombani, Spartaco M.,De Crescentini, Lucia,Giorgi, Raffaello,Monti, Susanna,Perrone, Ada,Perrulli, Francesca R.,Renzetti, Anna Rita,Santeusanio, Stefania

, p. 64 - 76 (2007/10/03)

Based on preliminary molecular modelling study, the synthesis of two different classes of biphenylyltetrazole derivatives of 1-aminopyrroles, as potentially active non-peptide angiotensin II (AII) antagonists, is reported. Some NH-Boc protected 1-aminopyr

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