Cas 41107-22-6,(2R,3R)‐3,5‐diacetoxy‐2‐(acetoxymethyl)‐2,3‐dihydro‐4H‐pyran‐4‐one

41107-22-6

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Basic information

Product Name: (2R,3R)‐3,5‐diacetoxy‐2‐(acetoxymethyl)‐2,3‐dihydro‐4H‐pyran‐4‐one
Synonyms: (2R,3R)‐3,5‐diacetoxy‐2‐(acetoxymethyl)‐2,3‐dihydro‐4H‐pyran‐4‐one
CAS NO:41107-22-6
Molecular Formula:
Molecular Weight: 286.238
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)‐3,5‐diacetoxy‐2‐(acetoxymethyl)‐2,3‐dihydro‐4H‐pyran‐4‐one(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R)‐3,5‐diacetoxy‐2‐(acetoxymethyl)‐2,3‐dihydro‐4H‐pyran‐4‐one(41107-22-6)
EPA Substance Registry System: (2R,3R)‐3,5‐diacetoxy‐2‐(acetoxymethyl)‐2,3‐dihydro‐4H‐pyran‐4‐one(41107-22-6)

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: 41107-22-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 41107-22-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,1,0 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 41107-22:
(7*4)+(6*1)+(5*1)+(4*0)+(3*7)+(2*2)+(1*2)=66
66 % 10 = 6
So 41107-22-6 is a valid CAS Registry Number.

41107-22-6Upstream product

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41107-22-6Relevant academic research and scientific papers

Chemo-enzymatic three-step conversion of glucose to kojic acid

Lassfolk, Robert,Suonpa?, Anu,Birikh, Klara,Leino, Reko

, p. 14737 - 14740 (2019)

Kojic acid is an important biomolecule, currently produced by fermentation and having a wide range of potential applications. A faster and more direct chemical route could open the door for its large-scale production and wider utilization in biorefineries. Here we describe an efficient method for the preparation of kojic acid from d-glucose via glucosone by a three-step chemo-enzymatic route.

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