Cas 862205-06-9,4-[5-(<i>tert</i>-butyl-diphenyl-silanyloxy)-4-dimethylamino-6-methyl-5,6-dihydro-4<i>H</i>-pyran-2-yl]-4-hydroxy-cyclohexa-2,5-dienone

862205-06-9

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Basic information

Product Name: 4-[5-(tert-butyl-diphenyl-silanyloxy)-4-dimethylamino-6-methyl-5,6-dihydro-4H-pyran-2-yl]-4-hydroxy-cyclohexa-2,5-dienone
Synonyms: 4-[5-(tert-butyl-diphenyl-silanyloxy)-4-dimethylamino-6-methyl-5,6-dihydro-4H-pyran-2-yl]-4-hydroxy-cyclohexa-2,5-dienone
CAS NO:862205-06-9
Molecular Formula:
Molecular Weight: 503.714
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: 4-[5-(tert-butyl-diphenyl-silanyloxy)-4-dimethylamino-6-methyl-5,6-dihydro-4H-pyran-2-yl]-4-hydroxy-cyclohexa-2,5-dienone(CAS DataBase Reference)
NIST Chemistry Reference: 4-[5-(tert-butyl-diphenyl-silanyloxy)-4-dimethylamino-6-methyl-5,6-dihydro-4H-pyran-2-yl]-4-hydroxy-cyclohexa-2,5-dienone(862205-06-9)
EPA Substance Registry System: 4-[5-(tert-butyl-diphenyl-silanyloxy)-4-dimethylamino-6-methyl-5,6-dihydro-4H-pyran-2-yl]-4-hydroxy-cyclohexa-2,5-dienone(862205-06-9)

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: 862205-06-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 862205-06-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,2,2,0 and 5 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 862205-06:
(8*8)+(7*6)+(6*2)+(5*2)+(4*0)+(3*5)+(2*0)+(1*6)=149
149 % 10 = 9
So 862205-06-9 is a valid CAS Registry Number.

862205-06-9Upstream product

862205-06-9Downstream Products

862205-06-9Relevant academic research and scientific papers

The "reverse polarity" approach to ravidomycin. Aryl C-aminoglycosides from a lithiated aminoglycal

Parker, Kathlyn A.,Su, Dai-Shi

, p. 187 - 197 (2007/10/03)

A three-step sequence affects the regio- and stereospecific elaboration of an aryl C-aminoglycoside from a simple aminoglycal and a quinone. Direct lithiation of the glycal followed by addition of the quinone, reduction of the quinol adduct, and hydrobora

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