Cas 41682-52-4,(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl cinnamate

41682-52-4

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Basic information

Product Name: (2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl cinnamate
Synonyms: (2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl cinnamate
CAS NO:41682-52-4
Molecular Formula:
Molecular Weight: 310.304
EINECS: N/A
Product Categories: N/A
Mol File: 41682-52-4.mol
Article Data: 2

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: (2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl cinnamate(CAS DataBase Reference)
NIST Chemistry Reference: (2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl cinnamate(41682-52-4)
EPA Substance Registry System: (2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-2-yl cinnamate(41682-52-4)

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: 41682-52-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 41682-52-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,6,8 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 41682-52:
(7*4)+(6*1)+(5*6)+(4*8)+(3*2)+(2*5)+(1*2)=114
114 % 10 = 4
So 41682-52-4 is a valid CAS Registry Number.

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41682-52-4Relevant articles and documents

Stereoselective synthesis of β-glycosyl esters of cis-cinnamic acid and its derivatives using unprotected glycosyl donors

Matsuo, Kazumasa,Nishikawa, Keisuke,Shindo, Mitsuru

experimental part, p. 5688 - 5692 (2011/11/06)

The β-glycosyl esters of cis-cinnamic acid were synthesized directly using Hannesian's unprotected glycosyl donor and the carboxylic acid in toluene. This protocol does not require protecting groups on the glycosyl donors, and high stereoselectivity was a

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