Cas 606128-77-2,(2R,3R,4R,5S,7S)-7-(tert-butyldimethylsilanyloxy)-2,3-dihydroxy-4-methyl-5-triisopropylsilanyloxycycloheptanone

606128-77-2

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Basic information

Product Name: (2R,3R,4R,5S,7S)-7-(tert-butyldimethylsilanyloxy)-2,3-dihydroxy-4-methyl-5-triisopropylsilanyloxycycloheptanone
Synonyms: (2R,3R,4R,5S,7S)-7-(tert-butyldimethylsilanyloxy)-2,3-dihydroxy-4-methyl-5-triisopropylsilanyloxycycloheptanone
CAS NO:606128-77-2
Molecular Formula:
Molecular Weight: 460.802
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,4R,5S,7S)-7-(tert-butyldimethylsilanyloxy)-2,3-dihydroxy-4-methyl-5-triisopropylsilanyloxycycloheptanone(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R,4R,5S,7S)-7-(tert-butyldimethylsilanyloxy)-2,3-dihydroxy-4-methyl-5-triisopropylsilanyloxycycloheptanone(606128-77-2)
EPA Substance Registry System: (2R,3R,4R,5S,7S)-7-(tert-butyldimethylsilanyloxy)-2,3-dihydroxy-4-methyl-5-triisopropylsilanyloxycycloheptanone(606128-77-2)

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: 606128-77-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 606128-77-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,6,1,2 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 606128-77:
(8*6)+(7*0)+(6*6)+(5*1)+(4*2)+(3*8)+(2*7)+(1*7)=142
142 % 10 = 2
So 606128-77-2 is a valid CAS Registry Number.

606128-77-2Upstream product

80522-42-5 triisopropylsilyl trifluoromethanesulfonate

606128-77-2Downstream Products

606128-77-2Relevant academic research and scientific papers

Functionality propagation by alkylative oxidation of cross-conjugated cycloheptadienyl sulfones

Torres, Eduardo,Chen, Yuzhong,Kim, In Chul,Fuchs

, p. 3124 - 3131 (2003)

Getting the most out of sulfur. Enantiopure epoxyvinyl sulfone 1 is transformed to syn- and anti-dienyl sulfones 2 and 3, respectively, by means of a nucleophilic methylation/sulfenylation/directed elimination reaction sequence. Compound 2 has been converted into termini-differentiated seven-carbon polypropionate segments found in five biologically significant natural products.

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