Cas 895533-69-4,(S)-1-({1-[((S)-1-{[1-(dimethylcarbamoyl)-1-methylethyl]carbamoyl}-2-phenylethoxy)carbonyl]-1-methylethyl}carbamoyl)-2-phenylethyl 2-[(2-hydroxyacetyl)amino]-2-methylpropanoate

895533-69-4

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Basic information

Product Name: (S)-1-({1-[((S)-1-{[1-(dimethylcarbamoyl)-1-methylethyl]carbamoyl}-2-phenylethoxy)carbonyl]-1-methylethyl}carbamoyl)-2-phenylethyl 2-[(2-hydroxyacetyl)amino]-2-methylpropanoate
Synonyms:
CAS NO:895533-69-4
Molecular Formula:
Molecular Weight: 654.761
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)-1-({1-[((S)-1-{[1-(dimethylcarbamoyl)-1-methylethyl]carbamoyl}-2-phenylethoxy)carbonyl]-1-methylethyl}carbamoyl)-2-phenylethyl 2-[(2-hydroxyacetyl)amino]-2-methylpropanoate(CAS DataBase Reference)
NIST Chemistry Reference: (S)-1-({1-[((S)-1-{[1-(dimethylcarbamoyl)-1-methylethyl]carbamoyl}-2-phenylethoxy)carbonyl]-1-methylethyl}carbamoyl)-2-phenylethyl 2-[(2-hydroxyacetyl)amino]-2-methylpropanoate(895533-69-4)
EPA Substance Registry System: (S)-1-({1-[((S)-1-{[1-(dimethylcarbamoyl)-1-methylethyl]carbamoyl}-2-phenylethoxy)carbonyl]-1-methylethyl}carbamoyl)-2-phenylethyl 2-[(2-hydroxyacetyl)amino]-2-methylpropanoate(895533-69-4)

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: 895533-69-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 895533-69-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,5,5,3 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 895533-69:
(8*8)+(7*9)+(6*5)+(5*5)+(4*3)+(3*3)+(2*6)+(1*9)=224
224 % 10 = 4
So 895533-69-4 is a valid CAS Registry Number.

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895533-69-4Relevant academic research and scientific papers

Synthesis of enniatin-like cyclic depsipeptides via 'direct amide cyclization'

Koettgen, Peter,Linden, Anthony,Heimgartner, Heinz

, p. 731 - 746 (2007/10/03)

The synthesis of several 18-membered cyclodepsipeptides with an alternating sequence of α,α-disubstituted α-amino acids and α-hydroxy acids (compounds 14a-14e) is described. The ring closure via macrolactonization was accomplished by treatment of a dilute

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