Cas 1326232-16-9,(3-(2-[4-(4-tert-butylbenzyl)piperazin-1-yl]-1-methyl-2-oxoethyl)phenyl)(phenyl)methanone

1326232-16-9

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Basic information

Product Name: (3-(2-[4-(4-tert-butylbenzyl)piperazin-1-yl]-1-methyl-2-oxoethyl)phenyl)(phenyl)methanone
Synonyms: (3-(2-[4-(4-tert-butylbenzyl)piperazin-1-yl]-1-methyl-2-oxoethyl)phenyl)(phenyl)methanone
CAS NO:1326232-16-9
Molecular Formula:
Molecular Weight: 468.639
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-(2-[4-(4-tert-butylbenzyl)piperazin-1-yl]-1-methyl-2-oxoethyl)phenyl)(phenyl)methanone(CAS DataBase Reference)
NIST Chemistry Reference: (3-(2-[4-(4-tert-butylbenzyl)piperazin-1-yl]-1-methyl-2-oxoethyl)phenyl)(phenyl)methanone(1326232-16-9)
EPA Substance Registry System: (3-(2-[4-(4-tert-butylbenzyl)piperazin-1-yl]-1-methyl-2-oxoethyl)phenyl)(phenyl)methanone(1326232-16-9)

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: 1326232-16-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1326232-16-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,6,2,3 and 2 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1326232-16:
(9*1)+(8*3)+(7*2)+(6*6)+(5*2)+(4*3)+(3*2)+(2*1)+(1*6)=119
119 % 10 = 9
So 1326232-16-9 is a valid CAS Registry Number.

1326232-16-9Upstream product

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1326232-16-9Relevant academic research and scientific papers

Stable ester and amide conjugates of some NSAIDs as analgesic and antiinflammatory compounds with improved biological activity

Uludag, Mecit Orhan,Caliskan Erguen, Burcu,Alkan, Duygu Asli,Ercan, Niluefer,Oezkan, Gueler Yagmur,Banoglu, Erden

experimental part, p. 427 - 439 (2012/02/02)

A set of ester and amide derivatives of some acidic NSAIDs, including ibuprofen, ketoprofen, and mefenamic acid (1-3), were synthesized and evaluated for their in vivo analgesic and antiinflammatory activity using the p-benzoquinone-induced writhing test

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