Cas 41341-56-4,(2R,3R,4S,5R,6S)-2-(acetoxymethyl)-6-[(4-acetylphenyl)thio]tetrahydro-2H-pyran-3,4,5-triyl triacetate

41341-56-4

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Basic information

Product Name: (2R,3R,4S,5R,6S)-2-(acetoxymethyl)-6-[(4-acetylphenyl)thio]tetrahydro-2H-pyran-3,4,5-triyl triacetate
Synonyms: (2R,3R,4S,5R,6S)-2-(acetoxymethyl)-6-[(4-acetylphenyl)thio]tetrahydro-2H-pyran-3,4,5-triyl triacetate
CAS NO:41341-56-4
Molecular Formula:
Molecular Weight: 482.508
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,4S,5R,6S)-2-(acetoxymethyl)-6-[(4-acetylphenyl)thio]tetrahydro-2H-pyran-3,4,5-triyl triacetate(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R,4S,5R,6S)-2-(acetoxymethyl)-6-[(4-acetylphenyl)thio]tetrahydro-2H-pyran-3,4,5-triyl triacetate(41341-56-4)
EPA Substance Registry System: (2R,3R,4S,5R,6S)-2-(acetoxymethyl)-6-[(4-acetylphenyl)thio]tetrahydro-2H-pyran-3,4,5-triyl triacetate(41341-56-4)

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: 41341-56-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 41341-56-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,3,4 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 41341-56:
(7*4)+(6*1)+(5*3)+(4*4)+(3*1)+(2*5)+(1*6)=84
84 % 10 = 4
So 41341-56-4 is a valid CAS Registry Number.

41341-56-4Upstream product

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41341-56-4Relevant academic research and scientific papers

Palladium-catalyzed cross-coupling reaction of thioglycosides with (hetero)aryl halides

Brachet, Etienne,Brion, Jean-Daniel,Messaoudi, Samir,Alami, Mouad

, p. 477 - 490 (2013/05/08)

α- and β-thioglycosides serve as effective nucleophiles for Buchwald-Hartwig cross-coupling reactions using functionalized (hetero)aryl halides. The functional group tolerance on the electrophilic partner is typically high, both benzyl and acetate protect

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