Cas 870450-02-5,2-Pyridinecarboxylic acid, 5-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-butynyl]-, methyl ester

870450-02-5

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Basic information

Product Name: 2-Pyridinecarboxylic acid, 5-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-butynyl]-, methyl ester
Synonyms:
CAS NO:870450-02-5
Molecular Formula: C17H25NO3Si
Molecular Weight: 319.476
EINECS: N/A
Product Categories: N/A
Mol File: 870450-02-5.mol
Article Data: 1

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-Pyridinecarboxylic acid, 5-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-butynyl]-, methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-Pyridinecarboxylic acid, 5-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-butynyl]-, methyl ester(870450-02-5)
EPA Substance Registry System: 2-Pyridinecarboxylic acid, 5-[4-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-1-butynyl]-, methyl ester(870450-02-5)

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: 870450-02-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 870450-02-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,0,4,5 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 870450-02:
(8*8)+(7*7)+(6*0)+(5*4)+(4*5)+(3*0)+(2*0)+(1*2)=155
155 % 10 = 5
So 870450-02-5 is a valid CAS Registry Number.

870450-02-5Upstream product

870450-02-5Downstream Products

870450-02-5Relevant articles and documents

Ligand creation via linking - A rapid and convenient method for construction of novel supported PyOX-ligands

Oila, Markku J.,Tois, Jan E.,Koskinen, Ari M.P.

, p. 10748 - 10756 (2005)

A novel supported amino alcohol linker was synthesized and utilized for attachment of picolinic acid derivatives onto different supports. When the resin bound molecule was further activated, the PyOX-moiety could be constructed reliably in enantiopure form. Furthermore, an efficient Pd-catalyzed modification of a picolinic acid derivative is presented.

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