Cas 1403380-46-0,(2S,1’S) 2-{3-[1-(4-decyl-3-hydroxy-2-oxo-2,5-dihydro-1H-pyrrole-1-carbonyl)-2-methylpropyl]ureido}-3-phenylpropionic acid

1403380-46-0

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Basic information

Product Name: (2S,1’S) 2-{3-[1-(4-decyl-3-hydroxy-2-oxo-2,5-dihydro-1H-pyrrole-1-carbonyl)-2-methylpropyl]ureido}-3-phenylpropionic acid
Synonyms: (2S,1’S) 2-{3-[1-(4-decyl-3-hydroxy-2-oxo-2,5-dihydro-1H-pyrrole-1-carbonyl)-2-methylpropyl]ureido}-3-phenylpropionic acid
CAS NO:1403380-46-0
Molecular Formula:
Molecular Weight: 529.677
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: (2S,1’S) 2-{3-[1-(4-decyl-3-hydroxy-2-oxo-2,5-dihydro-1H-pyrrole-1-carbonyl)-2-methylpropyl]ureido}-3-phenylpropionic acid(CAS DataBase Reference)
NIST Chemistry Reference: (2S,1’S) 2-{3-[1-(4-decyl-3-hydroxy-2-oxo-2,5-dihydro-1H-pyrrole-1-carbonyl)-2-methylpropyl]ureido}-3-phenylpropionic acid(1403380-46-0)
EPA Substance Registry System: (2S,1’S) 2-{3-[1-(4-decyl-3-hydroxy-2-oxo-2,5-dihydro-1H-pyrrole-1-carbonyl)-2-methylpropyl]ureido}-3-phenylpropionic acid(1403380-46-0)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1403380-46-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1403380-46-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,3,3,8 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1403380-46:
(9*1)+(8*4)+(7*0)+(6*3)+(5*3)+(4*8)+(3*0)+(2*4)+(1*6)=120
120 % 10 = 0
So 1403380-46-0 is a valid CAS Registry Number.

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1403380-46-0Relevant academic research and scientific papers

Total synthesis of leopolic acid A, a natural 2,3-pyrrolidinedione with antimicrobial activity

Dhavan, Atul A.,Kaduskar, Rahul D.,Musso, Loana,Scaglioni, Leonardo,Martino, Piera Anna,Dallavalle, Sabrina

, p. 1624 - 1628 (2016)

The first total synthesis of leopolic acid A, a fungal metabolite with a rare 2,3-pyrrolidinedione nucleus linked to an ureido dipeptide, was designed and carried out. Crucial steps for the strategy include a Dieckmann cyclization to obtain the 2,3-pyrrolidinedione ring and a Wittig olefination to install the polymethylene chain. An oxazolidinone-containing leopolic acid A analogue was also synthesized. The antibacterial activity showed by both compounds suggests that they could be considered as promising candidates for future developments.

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