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[2-({(R)-(3,5-dichloro-4-methoxyphenyl)-[2-(3-hydroxyphenyl)acetylamino]acetyl}methylamino)-(3S)-3-(4-fluoro-3-nitrophenyl)propionylamino]-(R)-(4-methoxyphenyl)acetic acid methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

193074-08-7

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  • [2-({(R)-(3,5-dichloro-4-methoxyphenyl)-[2-(3-hydroxyphenyl)acetylamino]acetyl}methylamino)-(3S)-3-(4-fluoro-3-nitrophenyl)propionylamino]-(R)-(4-methoxyphenyl)acetic acid methyl ester

    Cas No: 193074-08-7

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  • [2-({(R)-(3,5-dichloro-4-methoxyphenyl)-[2-(3-hydroxyphenyl)acetylamino]acetyl}methylamino)-(3S)-3-(4-fluoro-3-nitrophenyl)propionylamino]-(R)-(4-methoxyphenyl)acetic acid methyl ester

    Cas No: 193074-08-7

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193074-08-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 193074-08-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,0,7 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 193074-08:
(8*1)+(7*9)+(6*3)+(5*0)+(4*7)+(3*4)+(2*0)+(1*8)=137
137 % 10 = 7
So 193074-08-7 is a valid CAS Registry Number.

193074-08-7Downstream Products

193074-08-7Relevant articles and documents

Synthetic studies towards the synthesis of western and eastern chloropeptin I, II subunits

Roussi, Georges,Gonzalez Zamora, Eduardo,Carbonnelle, Annie-Claude,Beugelmans, Rene

, p. 2041 - 2063 (2007/10/03)

The western subunit (16-membered ring) was synthesized by the intramolecular SNAr reaction while the first 16-membered ring compound was obtained as a model of the eastern subunit via an intramolecular Ni0 mediated coupling reaction.

Synthesis of a model of chloropeptins I, II western subunit by the intramolecular S(N)Ar based methodology

Roussi, Georges,Zamora, Eduardo Gonzalez,Carbonnelle, Annie-Claude,Beugelmans, Rene

, p. 4401 - 4404 (2007/10/03)

Formation of a biaryl ether bond between the termini of a tetrapeptide containing a highly racemization prone amino acid by the intramolecular SNAr reaction afforded two diastereomeric 16-membered macrocycles along with their respective atropoisomers. The (R,S,R) and its atropoisomer constituted model of chloropeptins I, II, western part.

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