Cas 917877-41-9,tert-butyl {(4-bromophenyl)[(E)-5-methylhex-2-enyloxy]amino}[(trifluoroacetyl)amino]acetate

917877-41-9

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Basic information

Product Name: tert-butyl {(4-bromophenyl)[(E)-5-methylhex-2-enyloxy]amino}[(trifluoroacetyl)amino]acetate
Synonyms: tert-butyl {(4-bromophenyl)[(E)-5-methylhex-2-enyloxy]amino}[(trifluoroacetyl)amino]acetate
CAS NO:917877-41-9
Molecular Formula:
Molecular Weight: 509.364
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: tert-butyl {(4-bromophenyl)[(E)-5-methylhex-2-enyloxy]amino}[(trifluoroacetyl)amino]acetate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl {(4-bromophenyl)[(E)-5-methylhex-2-enyloxy]amino}[(trifluoroacetyl)amino]acetate(917877-41-9)
EPA Substance Registry System: tert-butyl {(4-bromophenyl)[(E)-5-methylhex-2-enyloxy]amino}[(trifluoroacetyl)amino]acetate(917877-41-9)

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: 917877-41-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 917877-41-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,7,8,7 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 917877-41:
(8*9)+(7*1)+(6*7)+(5*8)+(4*7)+(3*7)+(2*4)+(1*1)=219
219 % 10 = 9
So 917877-41-9 is a valid CAS Registry Number.

917877-41-9Upstream product

910579-13-4 tert-butyl [(4-bromophenyl)(hydroxy)amino][(trifluoroacetyl)amino]acetate

917877-41-9Downstream Products

917877-41-9Relevant academic research and scientific papers

Aromatic nitro groups and their reactions with chelated ester enolates

Stolz, Daniel,Kazmaier, Uli,Pick, Rigobert

, p. 3341 - 3347 (2006)

Chelated amino acid ester enolates react with aromatic nitro compounds in a 1,3-addition mode at the nitro group giving amino acids bearing an aryl(hydroxy)amino side chain. Best results were obtained with trifluoroacetyl-protected glycinates. Two equivalents of enolate are necessary for complete conversion, because one equivalent is oxidized during the reaction. Georg Thieme Verlag Stuttgart.

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