Cas 727985-90-2,(2S)-2-[(trans-4-isopropyl-cyclohexanecarbonyl)amino]-3-[4-(2-(methylamino)ethoxy)phenyl]propionic acid methyl ester

727985-90-2

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Basic information

Product Name: (2S)-2-[(trans-4-isopropyl-cyclohexanecarbonyl)amino]-3-[4-(2-(methylamino)ethoxy)phenyl]propionic acid methyl ester
Synonyms: (2S)-2-[(trans-4-isopropyl-cyclohexanecarbonyl)amino]-3-[4-(2-(methylamino)ethoxy)phenyl]propionic acid methyl ester
CAS NO:727985-90-2
Molecular Formula:
Molecular Weight: 404.55
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: (2S)-2-[(trans-4-isopropyl-cyclohexanecarbonyl)amino]-3-[4-(2-(methylamino)ethoxy)phenyl]propionic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S)-2-[(trans-4-isopropyl-cyclohexanecarbonyl)amino]-3-[4-(2-(methylamino)ethoxy)phenyl]propionic acid methyl ester(727985-90-2)
EPA Substance Registry System: (2S)-2-[(trans-4-isopropyl-cyclohexanecarbonyl)amino]-3-[4-(2-(methylamino)ethoxy)phenyl]propionic acid methyl ester(727985-90-2)

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: 727985-90-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 727985-90-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,2,7,9,8 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 727985-90:
(8*7)+(7*2)+(6*7)+(5*9)+(4*8)+(3*5)+(2*9)+(1*0)=222
222 % 10 = 2
So 727985-90-2 is a valid CAS Registry Number.

727985-90-2Upstream product

727985-90-2Downstream Products

727985-93-5 C₂₈H₃₉N₃O₄

727985-90-2Relevant academic research and scientific papers

Insulin-releasing activity of a series of phenylalanine derivatives

Tang, Lei,Yu, Juanhong,Wu, Haoshu,Fan, Houxing,Yang, Yushe,Ji, Ruyun

, p. 1997 - 2003 (2008/12/22)

A series of phenylalanine derivatives were synthesized and their biological activities were evaluated. Compounds (S)-3 and (R)-3 exhibited more potent insulin-releasing activity than that of nateglinide, compound (S)-3 also showed insulin-sensitizing activity in vitro. Both compounds were tested for hypoglycemia effect in vivo.

ALANINES COMPOUNDS, METHOD OF PREPARING THEM AND THEIR USE

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Page/Page column 13, (2008/06/13)

The present invention provides alanine compounds of formula (I) or their salts: In the formula (I), the configuration of α ― Carbon atom of alanine is R or S; R1 is hydrogen, unsubstituted or substituted C1-6 alkyl, unsubstituted or

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