Cas 548437-26-9,(2S,3S,4R,5S,6S)-1-(p-methoxybenzyloxy)-7-triisopropyloxy-2,4,6-trimethylheptane-3,5-diol

548437-26-9

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Basic information

Product Name: (2S,3S,4R,5S,6S)-1-(p-methoxybenzyloxy)-7-triisopropyloxy-2,4,6-trimethylheptane-3,5-diol
Synonyms: (2S,3S,4R,5S,6S)-1-(p-methoxybenzyloxy)-7-triisopropyloxy-2,4,6-trimethylheptane-3,5-diol
CAS NO:548437-26-9
Molecular Formula:
Molecular Weight: 482.776
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,3S,4R,5S,6S)-1-(p-methoxybenzyloxy)-7-triisopropyloxy-2,4,6-trimethylheptane-3,5-diol(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3S,4R,5S,6S)-1-(p-methoxybenzyloxy)-7-triisopropyloxy-2,4,6-trimethylheptane-3,5-diol(548437-26-9)
EPA Substance Registry System: (2S,3S,4R,5S,6S)-1-(p-methoxybenzyloxy)-7-triisopropyloxy-2,4,6-trimethylheptane-3,5-diol(548437-26-9)

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: 548437-26-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 548437-26-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,4,8,4,3 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 548437-26:
(8*5)+(7*4)+(6*8)+(5*4)+(4*3)+(3*7)+(2*2)+(1*6)=179
179 % 10 = 9
So 548437-26-9 is a valid CAS Registry Number.

548437-26-9Upstream product

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548437-26-9Relevant academic research and scientific papers

Toward the synthesis of reidispongiolide a: stereocontrolled synthesis of the C17-C22 and C23-C35 degradation fragments.

Paterson, Ian,Ashton, Kate,Britton, Robert,Knust, Henner

, p. 1963 - 1966 (2007/10/03)

[structure: see text] By relying on the asymmetric aldol reactions of chiral ketones, a highly stereocontrolled synthesis of each of the C(17)-C(22) and C(23)-C(35) degradation fragments of reidispongiolide A has been achieved. This permits a configuratio

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