Cas 882172-48-7,(R)-3-{(R)-3-Benzyl-4-[(2S,4R)-4-benzyloxy-2-(3-guanidino-propyl)-pyrrolidin-1-yl]-4-oxo-butyl}-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester

882172-48-7

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Product Name: (R)-3-{(R)-3-Benzyl-4-[(2S,4R)-4-benzyloxy-2-(3-guanidino-propyl)-pyrrolidin-1-yl]-4-oxo-butyl}-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester
Synonyms: (R)-3-{(R)-3-Benzyl-4-[(2S,4R)-4-benzyloxy-2-(3-guanidino-propyl)-pyrrolidin-1-yl]-4-oxo-butyl}-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester
CAS NO:882172-48-7
Molecular Formula:
Molecular Weight: 667.892
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: (R)-3-{(R)-3-Benzyl-4-[(2S,4R)-4-benzyloxy-2-(3-guanidino-propyl)-pyrrolidin-1-yl]-4-oxo-butyl}-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-3-{(R)-3-Benzyl-4-[(2S,4R)-4-benzyloxy-2-(3-guanidino-propyl)-pyrrolidin-1-yl]-4-oxo-butyl}-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester(882172-48-7)
EPA Substance Registry System: (R)-3-{(R)-3-Benzyl-4-[(2S,4R)-4-benzyloxy-2-(3-guanidino-propyl)-pyrrolidin-1-yl]-4-oxo-butyl}-3,4-dihydro-1H-isoquinoline-2-carboxylic acid tert-butyl ester(882172-48-7)

Safety Data

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Safety Statements: N/A
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RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 882172-48-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 882172-48-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,2,1,7 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 882172-48:
(8*8)+(7*8)+(6*2)+(5*1)+(4*7)+(3*2)+(2*4)+(1*8)=187
187 % 10 = 7
So 882172-48-7 is a valid CAS Registry Number.

882172-48-7Upstream product

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882172-48-7Relevant academic research and scientific papers

Synthesis of Tic-D-Phe Ψ[CH2-CH2] isostere and its use in the development of melanocortin receptor agonists

Tian, Xinrong,Chen, Xuemei,Gan, Lixian,Hayes, Jeffery C.,Switzer, Adrian G.,Solinsky, Mark G.,Ebetino, Frank H.,Wos, John A.,Pinney, Beth B.,Farmer, Julie A.,Crossdoersen, Doreen,Sheldon, Russell J.

, p. 1721 - 1725 (2007/10/03)

The first synthesis of Tic-d-Phe Ψ[CH2-CH2] isostere is described, which features diastereoselective alkylation of the tricyclic lactam 14. The use of this novel dipeptide isostere in the development of melanocortin agonists has been

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