Cas 80680-98-4,(S)-6-Benzyloxycarbonylamino-2-[(R)-2-(2-benzyloxycarbonylamino-acetylamino)-4-methyl-pentanoylamino]-hexanoic acid benzyl ester

80680-98-4

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Basic information

Product Name: (S)-6-Benzyloxycarbonylamino-2-[(R)-2-(2-benzyloxycarbonylamino-acetylamino)-4-methyl-pentanoylamino]-hexanoic acid benzyl ester
Synonyms:
CAS NO:80680-98-4
Molecular Formula:
Molecular Weight: 674.794
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)-6-Benzyloxycarbonylamino-2-[(R)-2-(2-benzyloxycarbonylamino-acetylamino)-4-methyl-pentanoylamino]-hexanoic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-6-Benzyloxycarbonylamino-2-[(R)-2-(2-benzyloxycarbonylamino-acetylamino)-4-methyl-pentanoylamino]-hexanoic acid benzyl ester(80680-98-4)
EPA Substance Registry System: (S)-6-Benzyloxycarbonylamino-2-[(R)-2-(2-benzyloxycarbonylamino-acetylamino)-4-methyl-pentanoylamino]-hexanoic acid benzyl ester(80680-98-4)

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: 80680-98-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 80680-98-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,6,8 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 80680-98:
(7*8)+(6*0)+(5*6)+(4*8)+(3*0)+(2*9)+(1*8)=144
144 % 10 = 4
So 80680-98-4 is a valid CAS Registry Number.

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80680-98-4Relevant academic research and scientific papers

THE DEPENDENCE OF ASYMMETRIC INDUCTION ON SOLVENT POLARITY AND TEMPERATURE IN PEPTIDE SYNTHESIS

Benoiton, N. Leo,Kuroda, K.,Chen, F. M. F.

, p. 3361 - 3364 (1981)

When a racemic 2,4-dialkyl-5(4H)-oxazolone reacts with an L-amino acid ester, the D-L epimer is formed in excess in apolar solvents and the L-L epimer is formed in excess in polar solvents, the proportion of L-L isomer increasing with decreasing temperature.

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