Cas 474882-23-0,(2R)-N-[(2R)-2-((1S,2E)-1-hydroxy-3-phenyl-2-propen-1-yl)-4-penten-1-oyl]bornane-10,2-sultam

474882-23-0

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Basic information

Product Name: (2R)-N-[(2R)-2-((1S,2E)-1-hydroxy-3-phenyl-2-propen-1-yl)-4-penten-1-oyl]bornane-10,2-sultam
Synonyms: (2R)-N-[(2R)-2-((1S,2E)-1-hydroxy-3-phenyl-2-propen-1-yl)-4-penten-1-oyl]bornane-10,2-sultam
CAS NO:474882-23-0
Molecular Formula:
Molecular Weight: 429.58
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: (2R)-N-[(2R)-2-((1S,2E)-1-hydroxy-3-phenyl-2-propen-1-yl)-4-penten-1-oyl]bornane-10,2-sultam(CAS DataBase Reference)
NIST Chemistry Reference: (2R)-N-[(2R)-2-((1S,2E)-1-hydroxy-3-phenyl-2-propen-1-yl)-4-penten-1-oyl]bornane-10,2-sultam(474882-23-0)
EPA Substance Registry System: (2R)-N-[(2R)-2-((1S,2E)-1-hydroxy-3-phenyl-2-propen-1-yl)-4-penten-1-oyl]bornane-10,2-sultam(474882-23-0)

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: 474882-23-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 474882-23-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,4,8,8 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 474882-23:
(8*4)+(7*7)+(6*4)+(5*8)+(4*8)+(3*2)+(2*2)+(1*3)=190
190 % 10 = 0
So 474882-23-0 is a valid CAS Registry Number.

474882-23-0Upstream product

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474882-23-0Relevant academic research and scientific papers

Synthesis of carbasugars from nucleophilic addition-ring closure (NARC)-derived cycloalkenes

Perlmutter, Patrick,Rose, Mark

, p. 1 - 10 (2002)

A short, enantioselective synthesis of carbasugars 4a-carba-α-L-xylofuranose 15, 4-epi-validatol 16 and their corresponding carboxylic acids 11 and 12 is reported. These compounds were prepared via a four-step sequence of nucleophilic addition, ring closu

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