Cas 899424-93-2,Benzenesulfonamide, N-(2-bromo-5-chloro-3-pyridinyl)-N-(methoxymethyl)-3-(trifluoromethyl)-

899424-93-2

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Basic information

Product Name: Benzenesulfonamide, N-(2-bromo-5-chloro-3-pyridinyl)-N-(methoxymethyl)-3-(trifluoromethyl)-
Synonyms:
CAS NO:899424-93-2
Molecular Formula: C14H11BrClF3N2O3S
Molecular Weight: 459.671
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: Benzenesulfonamide, N-(2-bromo-5-chloro-3-pyridinyl)-N-(methoxymethyl)-3-(trifluoromethyl)-(CAS DataBase Reference)
NIST Chemistry Reference: Benzenesulfonamide, N-(2-bromo-5-chloro-3-pyridinyl)-N-(methoxymethyl)-3-(trifluoromethyl)-(899424-93-2)
EPA Substance Registry System: Benzenesulfonamide, N-(2-bromo-5-chloro-3-pyridinyl)-N-(methoxymethyl)-3-(trifluoromethyl)-(899424-93-2)

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: 899424-93-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 899424-93-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,9,4,2 and 4 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 899424-93:
(8*8)+(7*9)+(6*9)+(5*4)+(4*2)+(3*4)+(2*9)+(1*3)=242
242 % 10 = 2
So 899424-93-2 is a valid CAS Registry Number.

899424-93-2Upstream product

899424-93-2Downstream Products

899424-93-2Relevant academic research and scientific papers

HETEROARYL SULFONAMIDES AND CCR2

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Page/Page column 140-141, (2008/06/13)

Compounds are provided that act as potent antagonists of the CCR2 receptor. Animal testing demonstrates that these compounds are useful for treating inflammation, a hallmark disease for CCR2. The compounds are generally aryl sulfonamide derivatives and are useful in pharmaceutical compositions, methods for the treatment of CCR2-mediated diseases, and as controls in assays for the identification of CCR2 antagonists.

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