Cas 865540-22-3,(2R,3R,5R,7S,8R)-3-Hydroxy-7-(4-methoxy-benzyloxy)-3,5-dimethyl-8-triisopropylsilanyloxymethyl-oxocane-2-carbaldehyde

865540-22-3

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Basic information

Product Name: (2R,3R,5R,7S,8R)-3-Hydroxy-7-(4-methoxy-benzyloxy)-3,5-dimethyl-8-triisopropylsilanyloxymethyl-oxocane-2-carbaldehyde
Synonyms: (2R,3R,5R,7S,8R)-3-Hydroxy-7-(4-methoxy-benzyloxy)-3,5-dimethyl-8-triisopropylsilanyloxymethyl-oxocane-2-carbaldehyde
CAS NO:865540-22-3
Molecular Formula:
Molecular Weight: 508.771
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,3R,5R,7S,8R)-3-Hydroxy-7-(4-methoxy-benzyloxy)-3,5-dimethyl-8-triisopropylsilanyloxymethyl-oxocane-2-carbaldehyde(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R,5R,7S,8R)-3-Hydroxy-7-(4-methoxy-benzyloxy)-3,5-dimethyl-8-triisopropylsilanyloxymethyl-oxocane-2-carbaldehyde(865540-22-3)
EPA Substance Registry System: (2R,3R,5R,7S,8R)-3-Hydroxy-7-(4-methoxy-benzyloxy)-3,5-dimethyl-8-triisopropylsilanyloxymethyl-oxocane-2-carbaldehyde(865540-22-3)

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: 865540-22-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 865540-22-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,5,5,4 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 865540-22:
(8*8)+(7*6)+(6*5)+(5*5)+(4*4)+(3*0)+(2*2)+(1*2)=183
183 % 10 = 3
So 865540-22-3 is a valid CAS Registry Number.

865540-22-3Upstream product

865540-22-3Downstream Products

865540-22-3Relevant academic research and scientific papers

A convergent coupling strategy for the formation of polycyclic ethers: Stereoselective synthesis of the BCDE fragment of brevetoxin A

Crimmins, Michael T.,McDougall, Patrick J.,Emmitte, Kyle A.

, p. 4033 - 4036 (2007/10/03)

(Chemical Equation Presented) A stereoselective synthesis of the BCDE fragment of brevetoxin A has been completed. anti-Glycolate aldol, glycolate alkylation, and ring-closing metathesis reactions were employed as key bond-forming events. A convergent ass

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