Cas 402598-61-2,N1,N5,N10,N14-tertakis[3-(4-acetoxyphenyl)-2-methyl-2-propenoyl]-1,5,10,14-tetraazatetradecane

402598-61-2

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Basic information

Product Name: N₁,N₅,N₁₀,N₁₄-tertakis[3-(4-acetoxyphenyl)-2-methyl-2-propenoyl]-1,5,10,14-tetraazatetradecane
Synonyms: N₁,N₅,N₁₀,N₁₄-tertakis[3-(4-acetoxyphenyl)-2-methyl-2-propenoyl]-1,5,10,14-tetraazatetradecane
CAS NO:402598-61-2
Molecular Formula:
Molecular Weight: 1011.18
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: N₁,N₅,N₁₀,N₁₄-tertakis[3-(4-acetoxyphenyl)-2-methyl-2-propenoyl]-1,5,10,14-tetraazatetradecane(CAS DataBase Reference)
NIST Chemistry Reference: N₁,N₅,N₁₀,N₁₄-tertakis[3-(4-acetoxyphenyl)-2-methyl-2-propenoyl]-1,5,10,14-tetraazatetradecane(402598-61-2)
EPA Substance Registry System: N₁,N₅,N₁₀,N₁₄-tertakis[3-(4-acetoxyphenyl)-2-methyl-2-propenoyl]-1,5,10,14-tetraazatetradecane(402598-61-2)

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: 402598-61-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 402598-61-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,2,5,9 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 402598-61:
(8*4)+(7*0)+(6*2)+(5*5)+(4*9)+(3*8)+(2*6)+(1*1)=142
142 % 10 = 2
So 402598-61-2 is a valid CAS Registry Number.

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402598-61-2Relevant academic research and scientific papers

A new nonpeptide tachykinin NK1 receptor antagonist isolated from the plants of compositae

Yamamoto, Atsushi,Nakamura, Ko,Furukawa, Kazuhito,Konishi, Yukari,Ogino, Takashi,Higashiura, Kunihiko,Yago, Hisashi,Okamoto, Kaoru,Otsuka, Masanori

, p. 47 - 52 (2002)

To find new tachykinin NK1 receptor antagonists from natural sources, we examined the tachykinin antagonist activity in the extracts of approximately 200 species of plants by the use of isolated guinea pig ileum. As a result, we discovered a no

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