Cas 626217-39-8,NH2CHCH2CH(CH3)2C6H3CF3N(CH2)4NCOCHCH2C6H3Cl2N(CH2)3CO

626217-39-8

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Basic information

Product Name: NH₂CHCH₂CH(CH₃)2C₆H₃CF₃N(CH₂)4NCOCHCH₂C₆H₃Cl₂N(CH₂)3CO
Synonyms: NH₂CHCH₂CH(CH₃)2C₆H₃CF₃N(CH₂)4NCOCHCH₂C₆H₃Cl₂N(CH₂)3CO
CAS NO:626217-39-8
Molecular Formula:
Molecular Weight: 599.524
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: NH₂CHCH₂CH(CH₃)2C₆H₃CF₃N(CH₂)4NCOCHCH₂C₆H₃Cl₂N(CH₂)3CO(CAS DataBase Reference)
NIST Chemistry Reference: NH₂CHCH₂CH(CH₃)2C₆H₃CF₃N(CH₂)4NCOCHCH₂C₆H₃Cl₂N(CH₂)3CO(626217-39-8)
EPA Substance Registry System: NH₂CHCH₂CH(CH₃)2C₆H₃CF₃N(CH₂)4NCOCHCH₂C₆H₃Cl₂N(CH₂)3CO(626217-39-8)

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: 626217-39-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 626217-39-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,6,2,1 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 626217-39:
(8*6)+(7*2)+(6*6)+(5*2)+(4*1)+(3*7)+(2*3)+(1*9)=148
148 % 10 = 8
So 626217-39-8 is a valid CAS Registry Number.

626217-39-8Upstream product

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626217-39-8Relevant academic research and scientific papers

Pyrrolidinones as orally bioavailable antagonists of the human melanocortin-4 receptor with anti-cachectic activity

Tran, Joe A.,Tucci, Fabio C.,Jiang, Wanlong,Marinkovic, Dragan,Chen, Caroline W.,Arellano, Melissa,Markison, Stacy,Fleck, Beth A.,Wen, Jenny,White, Nicole S.,Pontillo, Joseph,Saunders, John,Marks, Daniel,Hoare, Sam R.,Madan, Ajay,Foster, Alan C.,Chen, Chen

, p. 5166 - 5176 (2007)

A series of pyrrolidinones derived from phenylalanines were synthesized as potent antagonists of the human melanocortin-4 receptor. These compounds showed high potencies and selectivities, and several of them had good oral bioavailabilities. In addition,

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