Cas 149726-32-9,2-Methylsulfanyl-6-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-ylamino)-pyridine-3,4-dicarboxylic acid dimethyl ester

149726-32-9

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Basic information

Product Name: 2-Methylsulfanyl-6-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-ylamino)-pyridine-3,4-dicarboxylic acid dimethyl ester
Synonyms:
CAS NO:149726-32-9
Molecular Formula:
Molecular Weight: 586.574
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-Methylsulfanyl-6-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-ylamino)-pyridine-3,4-dicarboxylic acid dimethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-Methylsulfanyl-6-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-ylamino)-pyridine-3,4-dicarboxylic acid dimethyl ester(149726-32-9)
EPA Substance Registry System: 2-Methylsulfanyl-6-((2R,3R,4S,5R,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-ylamino)-pyridine-3,4-dicarboxylic acid dimethyl ester(149726-32-9)

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: 149726-32-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 149726-32-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,9,7,2 and 6 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 149726-32:
(8*1)+(7*4)+(6*9)+(5*7)+(4*2)+(3*6)+(2*3)+(1*2)=159
159 % 10 = 9
So 149726-32-9 is a valid CAS Registry Number.

149726-32-9Upstream product

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149726-32-9Relevant academic research and scientific papers

Aminopyrimidines as electron-rich azadienes: Extension of the synthetic potential of hetero Diels-Alder reactions under acidic conditions

García,Melguizo,Cobo,Sánchez,Nogueras,López,Low

, p. 57 - 60 (2007/10/03)

By addition of a catalytic amount of a strong acid and selection of the appropriate solvent, the cycloaddition reactions of dimethyl acetylenedicarboxylate (DMAD) to 6-aminopyrimidine derivatives drastically changed their course leading to new products, pyrrolo[3,4-c]pyridines, which were different from those obtained in the absence of acid. This change was interpreted on the basis of acid interception of the non-isolable adducts formed by initial hetero Diels-Alder cycloaddition between the reactants.

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