Cas 351412-74-3,[(2R,3R)-2,3-bis(tert-butyldimethylsilyloxy)-6-hydroxy-3-methyl-6-(1-(tert-butyldimethylsilyloxy)(2-naphthyl))hex-4-ynyl] (4-methylphenyl)sulfonate

351412-74-3

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Basic information

Product Name: [(2R,3R)-2,3-bis(tert-butyldimethylsilyloxy)-6-hydroxy-3-methyl-6-(1-(tert-butyldimethylsilyloxy)(2-naphthyl))hex-4-ynyl] (4-methylphenyl)sulfonate
Synonyms: [(2R,3R)-2,3-bis(tert-butyldimethylsilyloxy)-6-hydroxy-3-methyl-6-(1-(tert-butyldimethylsilyloxy)(2-naphthyl))hex-4-ynyl] (4-methylphenyl)sulfonate
CAS NO:351412-74-3
Molecular Formula:
Molecular Weight: 799.304
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)-2,3-bis(tert-butyldimethylsilyloxy)-6-hydroxy-3-methyl-6-(1-(tert-butyldimethylsilyloxy)(2-naphthyl))hex-4-ynyl] (4-methylphenyl)sulfonate(CAS DataBase Reference)
NIST Chemistry Reference: [(2R,3R)-2,3-bis(tert-butyldimethylsilyloxy)-6-hydroxy-3-methyl-6-(1-(tert-butyldimethylsilyloxy)(2-naphthyl))hex-4-ynyl] (4-methylphenyl)sulfonate(351412-74-3)
EPA Substance Registry System: [(2R,3R)-2,3-bis(tert-butyldimethylsilyloxy)-6-hydroxy-3-methyl-6-(1-(tert-butyldimethylsilyloxy)(2-naphthyl))hex-4-ynyl] (4-methylphenyl)sulfonate(351412-74-3)

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: 351412-74-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 351412-74-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,1,4,1 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 351412-74:
(8*3)+(7*5)+(6*1)+(5*4)+(4*1)+(3*2)+(2*7)+(1*4)=113
113 % 10 = 3
So 351412-74-3 is a valid CAS Registry Number.

351412-74-3Upstream product

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351412-74-3Relevant academic research and scientific papers

Selective intercalation of charge neutral intercalators into GG and CG steps: Implication of HOMO-LUMO interaction for sequence-selective drug intercalation into DNA

Nakatani,Matsuno,Adachi,Hagihara,Saito

, p. 5695 - 5702 (2007/10/03)

We have synthesized naphthopyranone epoxide 4 from D-isoascorbic acid together with its three diastereoisomers. DNA alkylation of ODNs containing 5′XGT3′ and 5′TGY3′ by 4 (11R, 13R), where X and Y are any nucleotide bases, occurred at all G residues excep

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