Cas 128541-01-5,2-Furancarbonsaeure-N-(2-phenyl-4-trifluormethylthiazol-5-yl)-amid

128541-01-5

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Basic information

Product Name: 2-Furancarbonsaeure-N-(2-phenyl-4-trifluormethylthiazol-5-yl)-amid
Synonyms: 2-Furancarbonsaeure-N-(2-phenyl-4-trifluormethylthiazol-5-yl)-amid
CAS NO:128541-01-5
Molecular Formula:
Molecular Weight: 338.31
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: 2-Furancarbonsaeure-N-(2-phenyl-4-trifluormethylthiazol-5-yl)-amid(CAS DataBase Reference)
NIST Chemistry Reference: 2-Furancarbonsaeure-N-(2-phenyl-4-trifluormethylthiazol-5-yl)-amid(128541-01-5)
EPA Substance Registry System: 2-Furancarbonsaeure-N-(2-phenyl-4-trifluormethylthiazol-5-yl)-amid(128541-01-5)

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: 128541-01-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 128541-01-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,8,5,4 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 128541-01:
(8*1)+(7*2)+(6*8)+(5*5)+(4*4)+(3*1)+(2*0)+(1*1)=115
115 % 10 = 5
So 128541-01-5 is a valid CAS Registry Number.

128541-01-5Upstream product

128541-01-5Downstream Products

128541-01-5Relevant academic research and scientific papers

5-Amino-4-trifluoromethylthiazoles and 5-Aminomethyl-4-trifluoromethyl-1,3-azoles: Useful Starting Materials for the Synthesis of Biologically Active Compounds

Burger, Klaus,Hoess, Eva,Geith, Klaus

, p. 360 - 365 (2007/10/02)

The title compounds are obtained from 5-fluoro-4-trifluoromethyl-1,3-azoles.Introduction of various side chains of potential biological interest at C-5 can be achieved with electrophiles by reaction of the amino group.

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