Cas 109449-66-3,ethyl 2-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)thio)benzoate

109449-66-3

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Basic information

Product Name: ethyl 2-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)thio)benzoate
Synonyms: ethyl 2-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)thio)benzoate
CAS NO:109449-66-3
Molecular Formula:
Molecular Weight: 344.386
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: ethyl 2-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)thio)benzoate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 2-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)thio)benzoate(109449-66-3)
EPA Substance Registry System: ethyl 2-(((2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl)thio)benzoate(109449-66-3)

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: 109449-66-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 109449-66-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,4,4 and 9 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 109449-66:
(8*1)+(7*0)+(6*9)+(5*4)+(4*4)+(3*9)+(2*6)+(1*6)=143
143 % 10 = 3
So 109449-66-3 is a valid CAS Registry Number.

109449-66-3Upstream product

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109449-66-3Relevant academic research and scientific papers

Nickel-catalyzed arylation, alkenylation, and alkynylation of unprotected thioglycosides at room temperature

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

supporting information, p. 15276 - 15280 (2013/11/06)

Unprotected thioglycosides were effective nucleophiles for Ni 0-catalyzed C-S bond-forming reaction with functionalized (hetero)aryl, alkenyl, and alkynyl halides. The functional-group tolerance on the electrophilic partner was typically high a

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