Cas 1154745-03-5,N-{3-[3-(3-bromo-5-tert-butyl-2-methoxyanilino)-5-tertbutyl-2-methoxyanilino]-5-tert-butyl-2-methoxyphenyl}-N',N'-di(tert-buthoxycarbonyl)-5-tert-butyl-2-methoxy-1,3-phenylenediamine

1154745-03-5

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Basic information

Product Name: N-{3-[3-(3-bromo-5-tert-butyl-2-methoxyanilino)-5-tertbutyl-2-methoxyanilino]-5-tert-butyl-2-methoxyphenyl}-N',N'-di(tert-buthoxycarbonyl)-5-tert-butyl-2-methoxy-1,3-phenylenediamine
Synonyms:
CAS NO:1154745-03-5
Molecular Formula:
Molecular Weight: 990.131
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: N-{3-[3-(3-bromo-5-tert-butyl-2-methoxyanilino)-5-tertbutyl-2-methoxyanilino]-5-tert-butyl-2-methoxyphenyl}-N',N'-di(tert-buthoxycarbonyl)-5-tert-butyl-2-methoxy-1,3-phenylenediamine(CAS DataBase Reference)
NIST Chemistry Reference: N-{3-[3-(3-bromo-5-tert-butyl-2-methoxyanilino)-5-tertbutyl-2-methoxyanilino]-5-tert-butyl-2-methoxyphenyl}-N',N'-di(tert-buthoxycarbonyl)-5-tert-butyl-2-methoxy-1,3-phenylenediamine(1154745-03-5)
EPA Substance Registry System: N-{3-[3-(3-bromo-5-tert-butyl-2-methoxyanilino)-5-tertbutyl-2-methoxyanilino]-5-tert-butyl-2-methoxyphenyl}-N',N'-di(tert-buthoxycarbonyl)-5-tert-butyl-2-methoxy-1,3-phenylenediamine(1154745-03-5)

Safety Data

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Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1154745-03-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1154745-03-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,4,7,4 and 5 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1154745-03:
(9*1)+(8*1)+(7*5)+(6*4)+(5*7)+(4*4)+(3*5)+(2*0)+(1*3)=145
145 % 10 = 5
So 1154745-03-5 is a valid CAS Registry Number.

1154745-03-5Upstream product

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1154745-03-5Relevant academic research and scientific papers

Azacalix[4]arene tetramethyl ether with inherent chirality generated by substitution on the nitrogen bridges

Ishibashi, Koichi,Tsue, Hirohito,Takahashi, Hiroki,Tamura, Rui

experimental part, p. 375 - 380 (2009/08/15)

The first inherently chiral azacalix[4]arene has been prepared by introducing three benzyl groups onto the nitrogen bridges. The highly enantioenriched compound was easily obtained via a moderately enantioselective cyclization followed by a simple crystal

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