Cas 108276-31-9,(2,2-Diethyl-5-methyl-4-oxo-[1,3]dioxan-5-yl)-carbamic acid benzyl ester

108276-31-9

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Basic information

Product Name: (2,2-Diethyl-5-methyl-4-oxo-[1,3]dioxan-5-yl)-carbamic acid benzyl ester
Synonyms: (2,2-Diethyl-5-methyl-4-oxo-[1,3]dioxan-5-yl)-carbamic acid benzyl ester
CAS NO:108276-31-9
Molecular Formula:
Molecular Weight: 321.373
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: (2,2-Diethyl-5-methyl-4-oxo-[1,3]dioxan-5-yl)-carbamic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2,2-Diethyl-5-methyl-4-oxo-[1,3]dioxan-5-yl)-carbamic acid benzyl ester(108276-31-9)
EPA Substance Registry System: (2,2-Diethyl-5-methyl-4-oxo-[1,3]dioxan-5-yl)-carbamic acid benzyl ester(108276-31-9)

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: 108276-31-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 108276-31-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,2,7 and 6 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 108276-31:
(8*1)+(7*0)+(6*8)+(5*2)+(4*7)+(3*6)+(2*3)+(1*1)=119
119 % 10 = 9
So 108276-31-9 is a valid CAS Registry Number.

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108276-31-9Relevant academic research and scientific papers

One Step Synthesis of 5-Acylamino-2,2-dialkyl-4-oxo-1,3-dioxanes: A Cyclic System Enabling Simultaneous Protection of Hydroxyl and Carboxyl Functions in α-Hydroxymethyl-α-Amino Acids

Kaminski, Z. J.,Leplawy, M. T.

, p. 649 - 651 (1986)

N-Acyl-α-alkylserines 1 were heated with aliphatic acetals 2 in the presence of mineral acid to afford 5-acylamino-2,2-dialkyl-4-oxo-1,3-dioxanes 3.This cyclic system is stable enough to survive amino group deprotection as well as peptide coupling conditi

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