Cas 393569-75-0,(RS)-4-(7-Phenyl-heptanoylamino)-5-[4-(pyridin-2-ylmethoxy)-phenyl]-pentanoic acid methyl ester

393569-75-0

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Basic information

Product Name: (RS)-4-(7-Phenyl-heptanoylamino)-5-[4-(pyridin-2-ylmethoxy)-phenyl]-pentanoic acid methyl ester
Synonyms: (RS)-4-(7-Phenyl-heptanoylamino)-5-[4-(pyridin-2-ylmethoxy)-phenyl]-pentanoic acid methyl ester
CAS NO:393569-75-0
Molecular Formula:
Molecular Weight: 502.654
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: (RS)-4-(7-Phenyl-heptanoylamino)-5-[4-(pyridin-2-ylmethoxy)-phenyl]-pentanoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (RS)-4-(7-Phenyl-heptanoylamino)-5-[4-(pyridin-2-ylmethoxy)-phenyl]-pentanoic acid methyl ester(393569-75-0)
EPA Substance Registry System: (RS)-4-(7-Phenyl-heptanoylamino)-5-[4-(pyridin-2-ylmethoxy)-phenyl]-pentanoic acid methyl ester(393569-75-0)

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: 393569-75-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 393569-75-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,3,5,6 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 393569-75:
(8*3)+(7*9)+(6*3)+(5*5)+(4*6)+(3*9)+(2*7)+(1*5)=200
200 % 10 = 0
So 393569-75-0 is a valid CAS Registry Number.

393569-75-0Upstream product

393569-74-9 (RS)-5-(4-Hydroxy-phenyl)-4-(7-phenyl-heptanoylamino)-pentanoic acid methyl ester

393569-75-0Downstream Products

393569-78-3 (RS)-4-(7-Phenyl-heptanoylamino)-5-[4-(pyridin-2-ylmethoxy)-phenyl]-pentanoic acid

393569-75-0Relevant academic research and scientific papers

Compounds and inhibitors of phospholipases

-

, (2008/06/13)

The present invention relates generally to amino acid derivatives and to methods of making the same. In particular, the invention relates to compounds bearing a stereochemical identity, that is, the same stereochemistry, with the chiral α-carbon of D-α-amino acids and their use in methods of therapy, including the treatment of inflammatory diseases, and to compositions and enantiomeric mixtures containing them.

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