Cas 1233959-65-3,((2R,3S,6S)-3-hydroxy-6-phenyl-3,6-dihydro-2H-pyran-2-yl)methyl 4-methylbenzenesulfonate

1233959-65-3

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Basic information

Product Name: ((2R,3S,6S)-3-hydroxy-6-phenyl-3,6-dihydro-2H-pyran-2-yl)methyl 4-methylbenzenesulfonate
Synonyms: ((2R,3S,6S)-3-hydroxy-6-phenyl-3,6-dihydro-2H-pyran-2-yl)methyl 4-methylbenzenesulfonate
CAS NO:1233959-65-3
Molecular Formula:
Molecular Weight: 360.431
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,3S,6S)-3-hydroxy-6-phenyl-3,6-dihydro-2H-pyran-2-yl)methyl 4-methylbenzenesulfonate(CAS DataBase Reference)
NIST Chemistry Reference: ((2R,3S,6S)-3-hydroxy-6-phenyl-3,6-dihydro-2H-pyran-2-yl)methyl 4-methylbenzenesulfonate(1233959-65-3)
EPA Substance Registry System: ((2R,3S,6S)-3-hydroxy-6-phenyl-3,6-dihydro-2H-pyran-2-yl)methyl 4-methylbenzenesulfonate(1233959-65-3)

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: 1233959-65-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1233959-65-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,3,9,5 and 9 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1233959-65:
(9*1)+(8*2)+(7*3)+(6*3)+(5*9)+(4*5)+(3*9)+(2*6)+(1*5)=173
173 % 10 = 3
So 1233959-65-3 is a valid CAS Registry Number.

1233959-65-3Upstream product

1233959-65-3Downstream Products

1233959-66-4 (2R,3S,6S)-2-(azidomethyl)-6-phenyl-3,6-dihydro-2H-pyran-3-ol

1233959-65-3Relevant academic research and scientific papers

Skeletal diversity via cationic rearrangements of substituted dihydropyrans

Medeiros, Matthew R.,Narayan, Radha S.,McDougal, Nolan T.,Schaus, Scott E.,Porco Jr., John A.

supporting information; experimental part, p. 3222 - 3225 (2010/10/05)

(Figure Presented) Substituted dihydropyrans, easily accessed from a commercially available glycal, undergo acid-catalyzed rearrangement to provide highly functionalized isochroman and dioxabicyclooctane scaffolds.

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