Cas 110261-71-7,benzyl c-6-(dimethoxymethyl)-3,4,5,6-tetrahydro-t-4,t-5-dihydroxy-r-3-methyl-2H-1,2-oxazine-2-carboxylate diacetate

110261-71-7

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Basic information

Product Name: benzyl c-6-(dimethoxymethyl)-3,4,5,6-tetrahydro-t-4,t-5-dihydroxy-r-3-methyl-2H-1,2-oxazine-2-carboxylate diacetate
Synonyms:
CAS NO:110261-71-7
Molecular Formula:
Molecular Weight: 425.436
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: benzyl c-6-(dimethoxymethyl)-3,4,5,6-tetrahydro-t-4,t-5-dihydroxy-r-3-methyl-2H-1,2-oxazine-2-carboxylate diacetate(CAS DataBase Reference)
NIST Chemistry Reference: benzyl c-6-(dimethoxymethyl)-3,4,5,6-tetrahydro-t-4,t-5-dihydroxy-r-3-methyl-2H-1,2-oxazine-2-carboxylate diacetate(110261-71-7)
EPA Substance Registry System: benzyl c-6-(dimethoxymethyl)-3,4,5,6-tetrahydro-t-4,t-5-dihydroxy-r-3-methyl-2H-1,2-oxazine-2-carboxylate diacetate(110261-71-7)

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: 110261-71-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 110261-71-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,2,6 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 110261-71:
(8*1)+(7*1)+(6*0)+(5*2)+(4*6)+(3*1)+(2*7)+(1*1)=67
67 % 10 = 7
So 110261-71-7 is a valid CAS Registry Number.

110261-71-7Upstream product

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110261-71-7Relevant academic research and scientific papers

Syntheses of Amino-dideoxyallose and Amino-deoxyribose Derivatives Using Acylnitroso Dienophiles

Defoin, Albert,Fritz, Hans,Geffroy, Guillaume,Streith, Jacques

, p. 1642 - 1658 (2007/10/02)

The dimethyl acetals 4 of (E)-2,4-pentadienal and of (E,E)- and (E,Z)-2,4-hexadienals undergo regio- and stereospecific cycloaddition reactions with in-situ-generated acylnitroso dienophiles 5a and 5b, leading thereby to the corresponding dihydrooxazines

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