Cas 1113057-33-2,2-{4-[2-(5-(amino(imino)methylamino)-1-oxo-2,3-dihydro-1H-benzo[c]azol-2-yl)-acetyl]-phenoxy}-acetic acid

1113057-33-2

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Basic information

Product Name: 2-{4-[2-(5-(amino(imino)methylamino)-1-oxo-2,3-dihydro-1H-benzo[c]azol-2-yl)-acetyl]-phenoxy}-acetic acid
Synonyms: 2-{4-[2-(5-(amino(imino)methylamino)-1-oxo-2,3-dihydro-1H-benzo[c]azol-2-yl)-acetyl]-phenoxy}-acetic acid
CAS NO:1113057-33-2
Molecular Formula:
Molecular Weight: 382.376
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: 2-{4-[2-(5-(amino(imino)methylamino)-1-oxo-2,3-dihydro-1H-benzo[c]azol-2-yl)-acetyl]-phenoxy}-acetic acid(CAS DataBase Reference)
NIST Chemistry Reference: 2-{4-[2-(5-(amino(imino)methylamino)-1-oxo-2,3-dihydro-1H-benzo[c]azol-2-yl)-acetyl]-phenoxy}-acetic acid(1113057-33-2)
EPA Substance Registry System: 2-{4-[2-(5-(amino(imino)methylamino)-1-oxo-2,3-dihydro-1H-benzo[c]azol-2-yl)-acetyl]-phenoxy}-acetic acid(1113057-33-2)

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: 1113057-33-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1113057-33-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,3,0,5 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1113057-33:
(9*1)+(8*1)+(7*1)+(6*3)+(5*0)+(4*5)+(3*7)+(2*3)+(1*3)=92
92 % 10 = 2
So 1113057-33-2 is a valid CAS Registry Number.

1113057-33-2Upstream product

1113057-19-4 benzyl 2-{4-[2-(5-(2,3-dicarbobenzoxy-1-guanidino)-1-oxo-2,3-dihydro-1H-benzo[c]azol-2-yl)acetyl]phenoxy}-acetate

1113057-33-2Downstream Products

1113057-33-2Relevant academic research and scientific papers

Guanidino substituted isoindolones as novel glycoprotein IIb-IIIa receptor antagonists

Lal, Bansi,Gangopadhyay, Ashok K.,Jagtap,Tanpure, Rajendra,Rao,Gupte, Ravindra D.,Subbarayan,Asudani, Gope

, p. 1815 - 1832 (2008/09/18)

Design and synthesis of a novel potent glycoprotein IIb-IIIa (GP IIb-IIIa) receptor antagonist based on isoindolone skeleton has been described. This scaffold has been derived from earlier reported pseudopeptides. Synthesis by a novel route has been achieved. Few molecules show very potent in vitro activity. Further identification of probable additional hydrogen bond donor site has been described.

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