Cas 199522-75-3,1-{3-[(5-bromo-pyridin-2-yl)-(3,4-dichloro-benzyl)-amino]-propyl}-3-[4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyl]-thiourea

199522-75-3

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Product Name: 1-{3-[(5-bromo-pyridin-2-yl)-(3,4-dichloro-benzyl)-amino]-propyl}-3-[4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyl]-thiourea
Synonyms: 1-{3-[(5-bromo-pyridin-2-yl)-(3,4-dichloro-benzyl)-amino]-propyl}-3-[4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyl]-thiourea
CAS NO:199522-75-3
Molecular Formula:
Molecular Weight: 649.439
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: 1-{3-[(5-bromo-pyridin-2-yl)-(3,4-dichloro-benzyl)-amino]-propyl}-3-[4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyl]-thiourea(CAS DataBase Reference)
NIST Chemistry Reference: 1-{3-[(5-bromo-pyridin-2-yl)-(3,4-dichloro-benzyl)-amino]-propyl}-3-[4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyl]-thiourea(199522-75-3)
EPA Substance Registry System: 1-{3-[(5-bromo-pyridin-2-yl)-(3,4-dichloro-benzyl)-amino]-propyl}-3-[4-(1,3-dioxo-1,3-dihydro-isoindol-2-yl)-butyl]-thiourea(199522-75-3)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 199522-75-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 199522-75-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,5,2 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 199522-75:
(8*1)+(7*9)+(6*9)+(5*5)+(4*2)+(3*2)+(2*7)+(1*5)=183
183 % 10 = 3
So 199522-75-3 is a valid CAS Registry Number.

199522-75-3Upstream product

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199522-75-3Relevant academic research and scientific papers

Nonpeptide somatostatin agonists with sst4 selectivity: Synthesis and structure-activity relationships of thioureas

Liu, Shenquan,Tang, Cheng,Ho, Bin,Ankersen, Michael,Stidsen, Carsten E.,Crider, A. Michael

, p. 4693 - 4705 (2007/10/03)

Utilizing NNC 26-9100 (11) as a structural lead, a variety of nonpeptide derivatives of somatostatin were synthesized and evaluated for sst2 and sst4 receptor binding affinity. A novel thiourea scaffold was utilized to attach (1) a h

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