Cas 603127-91-9,3-{[5-(4-aminomethyl-phenyl)-thiophene-2-carbonyl]-amino}-2-benzenesulfonylamino-propionic acid <i>tert</i>-butyl ester

603127-91-9

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Basic information

Product Name: 3-{[5-(4-aminomethyl-phenyl)-thiophene-2-carbonyl]-amino}-2-benzenesulfonylamino-propionic acid tert-butyl ester
Synonyms: 3-{[5-(4-aminomethyl-phenyl)-thiophene-2-carbonyl]-amino}-2-benzenesulfonylamino-propionic acid tert-butyl ester
CAS NO:603127-91-9
Molecular Formula:
Molecular Weight: 515.654
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: 3-{[5-(4-aminomethyl-phenyl)-thiophene-2-carbonyl]-amino}-2-benzenesulfonylamino-propionic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 3-{[5-(4-aminomethyl-phenyl)-thiophene-2-carbonyl]-amino}-2-benzenesulfonylamino-propionic acid tert-butyl ester(603127-91-9)
EPA Substance Registry System: 3-{[5-(4-aminomethyl-phenyl)-thiophene-2-carbonyl]-amino}-2-benzenesulfonylamino-propionic acid tert-butyl ester(603127-91-9)

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: 603127-91-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 603127-91-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,3,1,2 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 603127-91:
(8*6)+(7*0)+(6*3)+(5*1)+(4*2)+(3*7)+(2*9)+(1*1)=119
119 % 10 = 9
So 603127-91-9 is a valid CAS Registry Number.

603127-91-9Upstream product

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603127-91-9Relevant academic research and scientific papers

Thiophene-based vitronectin receptor antagonists

Bubenik, Monica,Meerovitch, Karen,Bergeron, Frederic,Attardo, Giorgio,Chan, Laval

, p. 503 - 506 (2007/10/03)

A series of αvβ3 antagonists based on a thiophene scaffold were synthesized via two routes and evaluated for in vitro biological activity. We have identified several structurally similar antagonists with different selectivities towards αIIbβ3, αvβ5 and α5β1 at the cellular level. In addition, these antagonists exerted an antiangiogenic effect in the chick chorioallantoic membrane (CAM) assay.

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