Cas 323196-47-0,{2-[3,5-dibromo-4-(3-octadecanoylamino-propoxy)-phenyl]-ethyl}-carbamic acid 1-biphenyl-4-yl-1-methyl-ethyl ester

323196-47-0

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Basic information

Product Name: {2-[3,5-dibromo-4-(3-octadecanoylamino-propoxy)-phenyl]-ethyl}-carbamic acid 1-biphenyl-4-yl-1-methyl-ethyl ester
Synonyms: {2-[3,5-dibromo-4-(3-octadecanoylamino-propoxy)-phenyl]-ethyl}-carbamic acid 1-biphenyl-4-yl-1-methyl-ethyl ester
CAS NO:323196-47-0
Molecular Formula:
Molecular Weight: 856.822
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: {2-[3,5-dibromo-4-(3-octadecanoylamino-propoxy)-phenyl]-ethyl}-carbamic acid 1-biphenyl-4-yl-1-methyl-ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {2-[3,5-dibromo-4-(3-octadecanoylamino-propoxy)-phenyl]-ethyl}-carbamic acid 1-biphenyl-4-yl-1-methyl-ethyl ester(323196-47-0)
EPA Substance Registry System: {2-[3,5-dibromo-4-(3-octadecanoylamino-propoxy)-phenyl]-ethyl}-carbamic acid 1-biphenyl-4-yl-1-methyl-ethyl ester(323196-47-0)

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: 323196-47-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 323196-47-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,3,1,9 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 323196-47:
(8*3)+(7*2)+(6*3)+(5*1)+(4*9)+(3*6)+(2*4)+(1*7)=130
130 % 10 = 0
So 323196-47-0 is a valid CAS Registry Number.

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323196-47-0Relevant academic research and scientific papers

Total synthesis of mololipids: A new series of anti-HIV moloka'iamine derivatives

Schoenfeld, Ryan C.,Lumb, Jean-Philip,Fantini, Jacques,Ganem, Bruce

, p. 2679 - 2681 (2000)

A new family of bioactive bromotyrosine derivatives, termed mololipids, was recently isolated from a Hawaiian sponge, but could not be resolved into individual components by chromatography. To complete their structural characterization and better understand structure-activity relationships, the first pure samples of dimyristoyl, distearoyl, dioleoyl, and stearoyl/oleoyl mololipids have now been prepared by total synthesis, and their anti-HIV activity investigated. (C) 2000 Published by Elsevier Science Ltd.

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