Cas 142477-99-4,8-benzyl-N-[(1S,2R,3S)-1-(cyclohexylmethyl)-3-cyclopropyl-2,3-dihydroxypropyl]-6-(3-pyridyl)-s-triazolo[4,3-a]pyrazine-3-acetamide

142477-99-4

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Basic information

Product Name: 8-benzyl-N-[(1S,2R,3S)-1-(cyclohexylmethyl)-3-cyclopropyl-2,3-dihydroxypropyl]-6-(3-pyridyl)-s-triazolo[4,3-a]pyrazine-3-acetamide
Synonyms:
CAS NO:142477-99-4
Molecular Formula:
Molecular Weight: 554.692
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: 8-benzyl-N-[(1S,2R,3S)-1-(cyclohexylmethyl)-3-cyclopropyl-2,3-dihydroxypropyl]-6-(3-pyridyl)-s-triazolo[4,3-a]pyrazine-3-acetamide(CAS DataBase Reference)
NIST Chemistry Reference: 8-benzyl-N-[(1S,2R,3S)-1-(cyclohexylmethyl)-3-cyclopropyl-2,3-dihydroxypropyl]-6-(3-pyridyl)-s-triazolo[4,3-a]pyrazine-3-acetamide(142477-99-4)
EPA Substance Registry System: 8-benzyl-N-[(1S,2R,3S)-1-(cyclohexylmethyl)-3-cyclopropyl-2,3-dihydroxypropyl]-6-(3-pyridyl)-s-triazolo[4,3-a]pyrazine-3-acetamide(142477-99-4)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 142477-99-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 142477-99-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,4,7 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 142477-99:
(8*1)+(7*4)+(6*2)+(5*4)+(4*7)+(3*7)+(2*9)+(1*9)=144
144 % 10 = 4
So 142477-99-4 is a valid CAS Registry Number.

142477-99-4Upstream product

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142477-99-4Relevant academic research and scientific papers

AMINO ACID DERIVATIVES USEFUL AS RENIN INHIBITORS

-

, (2008/06/13)

Compounds of the formula STR1 wherein A, B, X, Y, R 1, R 2, R 3, R 4 and R 5 are as set forth in the specification, in the form of optically pure diastereomers, mixtures of diastereomers, diastereomeric racemates or mixtures of diasteromeric racemates as well as pharmaceutically acceptable salts thereof which inhibit the activity of the natural enzyme renin and are useful in the control or prevention of high blood pressure and cardiac insufficiency are described.

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