Cas 195199-55-4,2-(3-benzyloxymethyl-3,4,5-trihydroxy-4-hydroxymethylpentyl)-2-methyl-1,3-dioxolane

195199-55-4

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Basic information

Product Name: 2-(3-benzyloxymethyl-3,4,5-trihydroxy-4-hydroxymethylpentyl)-2-methyl-1,3-dioxolane
Synonyms: 2-(3-benzyloxymethyl-3,4,5-trihydroxy-4-hydroxymethylpentyl)-2-methyl-1,3-dioxolane
CAS NO:195199-55-4
Molecular Formula:
Molecular Weight: 356.416
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: 2-(3-benzyloxymethyl-3,4,5-trihydroxy-4-hydroxymethylpentyl)-2-methyl-1,3-dioxolane(CAS DataBase Reference)
NIST Chemistry Reference: 2-(3-benzyloxymethyl-3,4,5-trihydroxy-4-hydroxymethylpentyl)-2-methyl-1,3-dioxolane(195199-55-4)
EPA Substance Registry System: 2-(3-benzyloxymethyl-3,4,5-trihydroxy-4-hydroxymethylpentyl)-2-methyl-1,3-dioxolane(195199-55-4)

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: 195199-55-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 195199-55-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,1,9 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 195199-55:
(8*1)+(7*9)+(6*5)+(5*1)+(4*9)+(3*9)+(2*5)+(1*5)=184
184 % 10 = 4
So 195199-55-4 is a valid CAS Registry Number.

195199-55-4Upstream product

190067-87-9 2-(3-benzyloxymethyl-3-hydroxy-4-hydroxymethylpent-4-enyl)-2-methyl-1,3-dioxolane

195199-55-4Downstream Products

195199-55-4Relevant academic research and scientific papers

The kinetics and thermodynamics of bicyclic ketal formation: An application to the synthesis of the zaragozic acids

Hegde, Sayee G.,Myles, David C.

, p. 11179 - 11190 (1997)

The kinetics and thermodynamics of ketalization of tetrahydroxyketones are examined in the synthesis of the ketal core of zaragozic acid Bx3.

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