Cas 121372-64-3,Benzoic acid 1-[(4R,5R)-1,3-dimethyl-4,5-bis-(3-trifluoromethyl-phenyl)-imidazolidin-2-yl]-hexyl ester

121372-64-3

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Basic information

Product Name: Benzoic acid 1-[(4R,5R)-1,3-dimethyl-4,5-bis-(3-trifluoromethyl-phenyl)-imidazolidin-2-yl]-hexyl ester
Synonyms:
CAS NO:121372-64-3
Molecular Formula:
Molecular Weight: 592.625
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: Benzoic acid 1-[(4R,5R)-1,3-dimethyl-4,5-bis-(3-trifluoromethyl-phenyl)-imidazolidin-2-yl]-hexyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid 1-[(4R,5R)-1,3-dimethyl-4,5-bis-(3-trifluoromethyl-phenyl)-imidazolidin-2-yl]-hexyl ester(121372-64-3)
EPA Substance Registry System: Benzoic acid 1-[(4R,5R)-1,3-dimethyl-4,5-bis-(3-trifluoromethyl-phenyl)-imidazolidin-2-yl]-hexyl ester(121372-64-3)

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: 121372-64-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 121372-64-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,3,7 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 121372-64:
(8*1)+(7*2)+(6*1)+(5*3)+(4*7)+(3*2)+(2*6)+(1*4)=93
93 % 10 = 3
So 121372-64-3 is a valid CAS Registry Number.

121372-64-3Upstream product

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121372-64-3Relevant academic research and scientific papers

Chiral Triflouro Diamines as Convenient Reagents for Determining the Enantiomeric Purity of Aldehydes by Use of 19F NMR Spectroscopy

Cuvinot, David,Mangeney, Pierre,Alexakis, Alexandre,Normant, Jean-F.,Lellouche, Jean-Paul

, p. 2420 - 2425 (2007/10/02)

N,N'-Dimethyl-1,2-bis-1,2-ethenediamines have been prepared.The meta trifluoro diamine was used as a chiral reagent for determining the enantiomeric purity of chiral aldehydes.

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