Cas 881853-90-3,2,2,2-trichloro-<i>N</i>-(4-chloro-phenyl)-<i>N</i>-(hexylcarbamoyl-phenyl-methyl)-acetamide

881853-90-3

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Basic information

Product Name: 2,2,2-trichloro-N-(4-chloro-phenyl)-N-(hexylcarbamoyl-phenyl-methyl)-acetamide
Synonyms: 2,2,2-trichloro-N-(4-chloro-phenyl)-N-(hexylcarbamoyl-phenyl-methyl)-acetamide
CAS NO:881853-90-3
Molecular Formula:
Molecular Weight: 490.257
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: 2,2,2-trichloro-N-(4-chloro-phenyl)-N-(hexylcarbamoyl-phenyl-methyl)-acetamide(CAS DataBase Reference)
NIST Chemistry Reference: 2,2,2-trichloro-N-(4-chloro-phenyl)-N-(hexylcarbamoyl-phenyl-methyl)-acetamide(881853-90-3)
EPA Substance Registry System: 2,2,2-trichloro-N-(4-chloro-phenyl)-N-(hexylcarbamoyl-phenyl-methyl)-acetamide(881853-90-3)

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: 881853-90-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 881853-90-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,1,8,5 and 3 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 881853-90:
(8*8)+(7*8)+(6*1)+(5*8)+(4*5)+(3*3)+(2*9)+(1*0)=213
213 % 10 = 3
So 881853-90-3 is a valid CAS Registry Number.

881853-90-3Upstream product

881853-90-3Downstream Products

881853-90-3Relevant academic research and scientific papers

A facile synthesis of 1,3,5-trisubstituted hydantoins via Ugi four-component condensation

Ignacio, José Miguel,Macho, Sonia,Marcaccini, Stefano,Pepino, Roberto,Torroba, Tomás

, p. 3051 - 3054 (2007/10/03)

A facile access to 1,3,5-trisubstituted hydantoins is achieved by combining an Ugi four-component condensation with a base-induced cyclization. This two-step sequence, which differs from any other method, is experimentally simple and allows a wide variety

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