Cas 857265-79-3,N-(5-bromo-1,3-thiazol-2-yl)-N'-[2-fluoro-5-(trifluoromethyl)phenyl]urea

857265-79-3

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Basic information

Product Name: N-(5-bromo-1,3-thiazol-2-yl)-N'-[2-fluoro-5-(trifluoromethyl)phenyl]urea
Synonyms: N-(5-bromo-1,3-thiazol-2-yl)-N'-[2-fluoro-5-(trifluoromethyl)phenyl]urea
CAS NO:857265-79-3
Molecular Formula:
Molecular Weight: 384.152
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-(5-bromo-1,3-thiazol-2-yl)-N'-[2-fluoro-5-(trifluoromethyl)phenyl]urea(CAS DataBase Reference)
NIST Chemistry Reference: N-(5-bromo-1,3-thiazol-2-yl)-N'-[2-fluoro-5-(trifluoromethyl)phenyl]urea(857265-79-3)
EPA Substance Registry System: N-(5-bromo-1,3-thiazol-2-yl)-N'-[2-fluoro-5-(trifluoromethyl)phenyl]urea(857265-79-3)

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: 857265-79-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 857265-79-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,7,2,6 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 857265-79:
(8*8)+(7*5)+(6*7)+(5*2)+(4*6)+(3*5)+(2*7)+(1*9)=213
213 % 10 = 3
So 857265-79-3 is a valid CAS Registry Number.

857265-79-3Upstream product

857265-79-3Downstream Products

857265-79-3Relevant academic research and scientific papers

PYRIMIDINES WITH TIE2 (TEK) ACTIVITY

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Page/Page column 119-120, (2010/02/12)

The invention relates to a compound of the Formula (I). or salt thereof wherein R1, R2, R3, R4, R5, R6, A, B, L, n and m are as defined in the description. The invention also relates to pharmaceutical compositions of said compounds, the use of said compounds as medicaments and in the production of an anti-angiogenic effect in a warm-blooded animal. The invention also relates to processes for the preparation of said compounds.

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