Cas 740807-41-4,Piperazine, 1-[[3-amino-4-(1,1-dimethylethyl)-1H-pyrazol-1-yl]acetyl]-4-(4-fluorophen yl)-

740807-41-4

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Basic information

Product Name: Piperazine, 1-[[3-amino-4-(1,1-dimethylethyl)-1H-pyrazol-1-yl]acetyl]-4-(4-fluorophen yl)-
Synonyms:
CAS NO:740807-41-4
Molecular Formula: C19H26FN5O
Molecular Weight: 359.447
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: Piperazine, 1-[[3-amino-4-(1,1-dimethylethyl)-1H-pyrazol-1-yl]acetyl]-4-(4-fluorophen yl)-(CAS DataBase Reference)
NIST Chemistry Reference: Piperazine, 1-[[3-amino-4-(1,1-dimethylethyl)-1H-pyrazol-1-yl]acetyl]-4-(4-fluorophen yl)-(740807-41-4)
EPA Substance Registry System: Piperazine, 1-[[3-amino-4-(1,1-dimethylethyl)-1H-pyrazol-1-yl]acetyl]-4-(4-fluorophen yl)-(740807-41-4)

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: 740807-41-4(Hazardous Substances Data)

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740807-41-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 740807-41-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,0,8,0 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 740807-41:
(8*7)+(7*4)+(6*0)+(5*8)+(4*0)+(3*7)+(2*4)+(1*1)=154
154 % 10 = 4
So 740807-41-4 is a valid CAS Registry Number.

740807-41-4Upstream product

740807-41-4Downstream Products

740807-41-4Relevant academic research and scientific papers

Substituted piperazines

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, (2008/06/13)

Compounds are provided that act as potent antagonists of the CCR1 receptor, and which have been further confirmed in animal testing for inflammation, one of the hallmark disease states for CCR1. The compounds are generally aryl piperazine derivatives and are useful in pharmaceutical compositions, methods for the treatment of CCR1-mediated diseases, and as controls in assays for the identification of competitive CCR1 antagonists.

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