Cas 597557-40-9,(-)-(1S,2R,3aR,5S,6aS)-5-(tert-butyldiphenylsilanyloxy)-1-ethynyl-2-(triethylsilanyloxy)octahydropentalene

597557-40-9

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Basic information

Product Name: (-)-(1S,2R,3aR,5S,6aS)-5-(tert-butyldiphenylsilanyloxy)-1-ethynyl-2-(triethylsilanyloxy)octahydropentalene
Synonyms: (-)-(1S,2R,3aR,5S,6aS)-5-(tert-butyldiphenylsilanyloxy)-1-ethynyl-2-(triethylsilanyloxy)octahydropentalene
CAS NO:597557-40-9
Molecular Formula:
Molecular Weight: 518.887
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: (-)-(1S,2R,3aR,5S,6aS)-5-(tert-butyldiphenylsilanyloxy)-1-ethynyl-2-(triethylsilanyloxy)octahydropentalene(CAS DataBase Reference)
NIST Chemistry Reference: (-)-(1S,2R,3aR,5S,6aS)-5-(tert-butyldiphenylsilanyloxy)-1-ethynyl-2-(triethylsilanyloxy)octahydropentalene(597557-40-9)
EPA Substance Registry System: (-)-(1S,2R,3aR,5S,6aS)-5-(tert-butyldiphenylsilanyloxy)-1-ethynyl-2-(triethylsilanyloxy)octahydropentalene(597557-40-9)

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: 597557-40-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 597557-40-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,9,7,5,5 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 597557-40:
(8*5)+(7*9)+(6*7)+(5*5)+(4*5)+(3*7)+(2*4)+(1*0)=219
219 % 10 = 9
So 597557-40-9 is a valid CAS Registry Number.

597557-40-9Upstream product

597557-40-9Downstream Products

597557-40-9Relevant academic research and scientific papers

Asymmetric synthesis of the highly potent anti-metastatic prostacyclin analogue cicaprost and its isomer isocicaprost

Lerm, Marco,Gais, Hans-Joachim,Cheng, Kejun,Vermeeren, Cornelia

, p. 9653 - 9667 (2007/10/03)

An asymmetric synthesis of the anti-metastatic prostacyclin analogue cicaprost and a formal one of its isomer isocicaprost by a new route are described. A key step of these syntheses is the coupling of a chiral bicyclic C6-C14 ethynyl building block with

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