Cas 1345465-86-2,methyl 2-[(tert-butoxycarbonyl)amino]-3,3,3-trifluoro-2-{[3-(4-nitrophenyl)isoxazol-5-yl]methyl}propanoate

1345465-86-2

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Basic information

Product Name: methyl 2-[(tert-butoxycarbonyl)amino]-3,3,3-trifluoro-2-{[3-(4-nitrophenyl)isoxazol-5-yl]methyl}propanoate
Synonyms: methyl 2-[(tert-butoxycarbonyl)amino]-3,3,3-trifluoro-2-{[3-(4-nitrophenyl)isoxazol-5-yl]methyl}propanoate
CAS NO:1345465-86-2
Molecular Formula:
Molecular Weight: 459.379
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: methyl 2-[(tert-butoxycarbonyl)amino]-3,3,3-trifluoro-2-{[3-(4-nitrophenyl)isoxazol-5-yl]methyl}propanoate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 2-[(tert-butoxycarbonyl)amino]-3,3,3-trifluoro-2-{[3-(4-nitrophenyl)isoxazol-5-yl]methyl}propanoate(1345465-86-2)
EPA Substance Registry System: methyl 2-[(tert-butoxycarbonyl)amino]-3,3,3-trifluoro-2-{[3-(4-nitrophenyl)isoxazol-5-yl]methyl}propanoate(1345465-86-2)

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: 1345465-86-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1345465-86-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,5,4,6 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1345465-86:
(9*1)+(8*3)+(7*4)+(6*5)+(5*4)+(4*6)+(3*5)+(2*8)+(1*6)=172
172 % 10 = 2
So 1345465-86-2 is a valid CAS Registry Number.

1345465-86-2Upstream product

1345465-86-2Downstream Products

1345465-95-3 methyl 2-amino-3,3,3-trifluoro-2-{[3-(4-nitrophenyl)isoxazol-5-yl]methyl}propanoate

1345465-86-2Relevant academic research and scientific papers

Click-chemistry approach to isoxazole-containing α-CF 3-substituted α-aminocarboxylates and α-aminophosphonates

Vorobyeva, Daria V.,Karimova, Natalya M.,Odinets, Irina L.,Roeschenthaler, Gerd-Volker,Osipov, Sergey N.

experimental part, p. 7335 - 7342 (2011/11/30)

A convenient strategy for the synthesis of isoxazole-containing α-CF3-substituted α-aminocarboxylates and α-aminophosphonates have been developed. The method is based on copper-catalyzed 1,3-dipolar cycloaddition of different aromatic nitrile o

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