Cas 895533-46-7,(-)-(S)-2-(2-benzyloxy-3-phenylpropanoylamino)-2-methylpropanoic acid

895533-46-7

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Basic information

Product Name: (-)-(S)-2-(2-benzyloxy-3-phenylpropanoylamino)-2-methylpropanoic acid
Synonyms: (-)-(S)-2-(2-benzyloxy-3-phenylpropanoylamino)-2-methylpropanoic acid
CAS NO:895533-46-7
Molecular Formula:
Molecular Weight: 341.407
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-(2-benzyloxy-3-phenylpropanoylamino)-2-methylpropanoic acid(CAS DataBase Reference)
NIST Chemistry Reference: (-)-(S)-2-(2-benzyloxy-3-phenylpropanoylamino)-2-methylpropanoic acid(895533-46-7)
EPA Substance Registry System: (-)-(S)-2-(2-benzyloxy-3-phenylpropanoylamino)-2-methylpropanoic acid(895533-46-7)

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: 895533-46-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 895533-46-7 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, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 895533-46:
(8*8)+(7*9)+(6*5)+(5*5)+(4*3)+(3*3)+(2*4)+(1*6)=217
217 % 10 = 7
So 895533-46-7 is a valid CAS Registry Number.

895533-46-7Upstream product

895533-33-2 (-)-(S)-2-benzyloxy-N-[1-methyl-1-(N-methyl-N-phenylcarbamoyl)ethyl]-3-phenylpropanamide

895533-46-7Downstream Products

895533-46-7Relevant academic research and scientific papers

Synthesis of a regular 24-membered cyclodepsipeptide by direct amide cyclization

K?ttgen, Peter,Linden, Anthony,Heimgartner, Heinz

experimental part, p. 689 - 698 (2009/12/26)

Aminoisobutyric Acid, Crystal Structure The synthesis of a 24-membered cyclic depsipeptide with an alternating sequence of phenyllactic acid and α-aminoisobutyric acid (Aib) is described. The linear precursor was prepared via the 'azirine/oxazolone method

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