Cas 181815-63-4,(S)-2-Amino-N-{4-[((S)-2-amino-3-methyl-butyrylamino)-methyl]-benzyl}-3-methyl-butyramide

181815-63-4

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Basic information

Product Name: (S)-2-Amino-N-{4-[((S)-2-amino-3-methyl-butyrylamino)-methyl]-benzyl}-3-methyl-butyramide
Synonyms: (S)-2-Amino-N-{4-[((S)-2-amino-3-methyl-butyrylamino)-methyl]-benzyl}-3-methyl-butyramide
CAS NO:181815-63-4
Molecular Formula:
Molecular Weight: 334.462
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-Amino-N-{4-[((S)-2-amino-3-methyl-butyrylamino)-methyl]-benzyl}-3-methyl-butyramide(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-Amino-N-{4-[((S)-2-amino-3-methyl-butyrylamino)-methyl]-benzyl}-3-methyl-butyramide(181815-63-4)
EPA Substance Registry System: (S)-2-Amino-N-{4-[((S)-2-amino-3-methyl-butyrylamino)-methyl]-benzyl}-3-methyl-butyramide(181815-63-4)

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: 181815-63-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 181815-63-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,8,1 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 181815-63:
(8*1)+(7*8)+(6*1)+(5*8)+(4*1)+(3*5)+(2*6)+(1*3)=144
144 % 10 = 4
So 181815-63-4 is a valid CAS Registry Number.

181815-63-4Upstream product

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181815-63-4Relevant academic research and scientific papers

Synthesis and structure of chiral macrocycles containing 2,2'-bipyridine subunits

Hopkins, R. Bruce,Albert, Jeffrey S.,Van Engen, Donna,Hamilton, Andrew D.

, p. 1121 - 1128 (2007/10/03)

A series of macrocyclic receptors has been prepared containing bipyridine groups linked to two amino acids. Variations in both the amino acid and the linking spacer have been made. The structure of the resulting macrocycles has been investigated using su

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