Cas 205063-79-2,(Z)-2-tert-Butoxycarbonylamino-3-{4'-[(Z)-2-methoxycarbonyl-2-(2-trimethylsilanyl-ethoxycarbonylamino)-vinyl]-biphenyl-4-yl}-acrylic acid benzyl ester

205063-79-2

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Basic information

Product Name: (Z)-2-tert-Butoxycarbonylamino-3-{4'-[(Z)-2-methoxycarbonyl-2-(2-trimethylsilanyl-ethoxycarbonylamino)-vinyl]-biphenyl-4-yl}-acrylic acid benzyl ester
Synonyms: (Z)-2-tert-Butoxycarbonylamino-3-{4'-[(Z)-2-methoxycarbonyl-2-(2-trimethylsilanyl-ethoxycarbonylamino)-vinyl]-biphenyl-4-yl}-acrylic acid benzyl ester
CAS NO:205063-79-2
Molecular Formula:
Molecular Weight: 672.85
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: (Z)-2-tert-Butoxycarbonylamino-3-{4'-[(Z)-2-methoxycarbonyl-2-(2-trimethylsilanyl-ethoxycarbonylamino)-vinyl]-biphenyl-4-yl}-acrylic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-2-tert-Butoxycarbonylamino-3-{4'-[(Z)-2-methoxycarbonyl-2-(2-trimethylsilanyl-ethoxycarbonylamino)-vinyl]-biphenyl-4-yl}-acrylic acid benzyl ester(205063-79-2)
EPA Substance Registry System: (Z)-2-tert-Butoxycarbonylamino-3-{4'-[(Z)-2-methoxycarbonyl-2-(2-trimethylsilanyl-ethoxycarbonylamino)-vinyl]-biphenyl-4-yl}-acrylic acid benzyl ester(205063-79-2)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 205063-79-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 205063-79-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,0,6 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 205063-79:
(8*2)+(7*0)+(6*5)+(5*0)+(4*6)+(3*3)+(2*7)+(1*9)=102
102 % 10 = 2
So 205063-79-2 is a valid CAS Registry Number.

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205063-79-2Relevant academic research and scientific papers

Synthesis of optically active arylene bis-alanine derivatives carrying orthogonal protecting groups

Ritzen, Andreas,Basu, Basudeb,Chattopadhyay, Shital K.,Dossa, Fahreen,Frejd, Torbjoern

, p. 503 - 512 (2007/10/03)

Derivatives of para- and meta-phenylene bis-alanine and related biphenyl systems, carrying four orthogonal protecting groups, were synthesised via combinations of Heck couplings and asymmetric hydrogenations. The intermediate unsaturated arylalanine derivatives were hydrogenated using [Rh(COD)((R,R)-DIPAMP)]+BF4- or [Rh(COD)(Me-DuPHOS)]+X- as catalysts to produce the optically active, protected amino acid derivatives in ≤98% e.e. as analysed by chiral phase HPLC.

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