Cas 176777-47-2,(S)-2-((1S,2S)-1-Aminomethyl-2-tert-butoxycarbonylamino-3-phenyl-propylamino)-4-methyl-pentanoic acid methyl ester

176777-47-2

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Basic information

Product Name: (S)-2-((1S,2S)-1-Aminomethyl-2-tert-butoxycarbonylamino-3-phenyl-propylamino)-4-methyl-pentanoic acid methyl ester
Synonyms:
CAS NO:176777-47-2
Molecular Formula:
Molecular Weight: 407.553
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: (S)-2-((1S,2S)-1-Aminomethyl-2-tert-butoxycarbonylamino-3-phenyl-propylamino)-4-methyl-pentanoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-((1S,2S)-1-Aminomethyl-2-tert-butoxycarbonylamino-3-phenyl-propylamino)-4-methyl-pentanoic acid methyl ester(176777-47-2)
EPA Substance Registry System: (S)-2-((1S,2S)-1-Aminomethyl-2-tert-butoxycarbonylamino-3-phenyl-propylamino)-4-methyl-pentanoic acid methyl ester(176777-47-2)

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: 176777-47-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 176777-47-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,6,7,7 and 7 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 176777-47:
(8*1)+(7*7)+(6*6)+(5*7)+(4*7)+(3*7)+(2*4)+(1*7)=192
192 % 10 = 2
So 176777-47-2 is a valid CAS Registry Number.

176777-47-2Upstream product

431063-61-5 Boc-PheψLeu-OMe

176777-47-2Downstream Products

176685-85-1 (S)-2-{(1S,2S)-1-[((S)-2-Benzyloxycarbonylamino-propionylamino)-methyl]-2-tert-butoxycarbonylamino-3-phenyl-propylamino}-4-methyl-pentanoic acid methyl ester

176777-47-2Relevant academic research and scientific papers

Branched peptides and conformationally constrained analogues from cyanomethyleneamino pseudopeptides

Suarez-Gea, M. Luisa,Garcia-Lopez, M. Teresa,Gonzalez-Muniz, Rosario,Herrero, Susana,Herranz, Rosario

, p. 2083 - 2084 (1996)

Catalytic hydrogenation of cyanomethyleneamino pseudopeptides, followed by peptide coupling and cyclization of the resulting aminomethyleneamino intermediates, gives access to branched and conformationally constrained peptide analogues.

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