Cas 705279-40-9,<i>N</i>,<i>N</i>-diethyl-4-[(4-hydroxy-phenyl)-(8-methyl-8-aza-bicyclo[3.2.1]oct-3-ylidene)-methyl]-benzamide

705279-40-9

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Basic information

Product Name: N,N-diethyl-4-[(4-hydroxy-phenyl)-(8-methyl-8-aza-bicyclo[3.2.1]oct-3-ylidene)-methyl]-benzamide
Synonyms:
CAS NO:705279-40-9
Molecular Formula:
Molecular Weight: 404.552
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: N,N-diethyl-4-[(4-hydroxy-phenyl)-(8-methyl-8-aza-bicyclo[3.2.1]oct-3-ylidene)-methyl]-benzamide(CAS DataBase Reference)
NIST Chemistry Reference: N,N-diethyl-4-[(4-hydroxy-phenyl)-(8-methyl-8-aza-bicyclo[3.2.1]oct-3-ylidene)-methyl]-benzamide(705279-40-9)
EPA Substance Registry System: N,N-diethyl-4-[(4-hydroxy-phenyl)-(8-methyl-8-aza-bicyclo[3.2.1]oct-3-ylidene)-methyl]-benzamide(705279-40-9)

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: 705279-40-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 705279-40-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,0,5,2,7 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 705279-40:
(8*7)+(7*0)+(6*5)+(5*2)+(4*7)+(3*9)+(2*4)+(1*0)=159
159 % 10 = 9
So 705279-40-9 is a valid CAS Registry Number.

705279-40-9Upstream product

705279-40-9Downstream Products

705279-40-9Relevant academic research and scientific papers

N,N-Dialkyl-4-[(8-azabicyclo[3.2.1]-oct-3-ylidene)phenylmethyl]benzamides, potent, selective δ opioid agonists

Carson, John R.,Coats, Steven J.,Codd, Ellen E.,Dax, Scott L.,Lee, Jung,Martinez, Rebecca P.,Neilson, Lou Anne,Pitis, Philip M.,Zhang, Sui-Po

, p. 2109 - 2112 (2007/10/03)

A series of N,N-dialkyl-4-(9-aryltropanylidenemethyl)benzamides was prepared. The lead compounds, 15a and 15c, exhibited extremely high affinity for the δ opioid receptor with excellent selectivity versus the μ opioid receptor. They were full agonists at

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