Cas 926893-05-2,Hexanoic acid, 6-[3-fluoro-4-[[[3-hydroxy-5-(hydroxymethyl)-2-methyl-4-pyridinyl]methyl] amino]phenoxy]-, ethyl ester

926893-05-2

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Basic information

Product Name: Hexanoic acid, 6-[3-fluoro-4-[[[3-hydroxy-5-(hydroxymethyl)-2-methyl-4-pyridinyl]methyl] amino]phenoxy]-, ethyl ester
Synonyms:
CAS NO:926893-05-2
Molecular Formula: C22H29FN2O5
Molecular Weight: 420.481
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: Hexanoic acid, 6-[3-fluoro-4-[[[3-hydroxy-5-(hydroxymethyl)-2-methyl-4-pyridinyl]methyl] amino]phenoxy]-, ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Hexanoic acid, 6-[3-fluoro-4-[[[3-hydroxy-5-(hydroxymethyl)-2-methyl-4-pyridinyl]methyl] amino]phenoxy]-, ethyl ester(926893-05-2)
EPA Substance Registry System: Hexanoic acid, 6-[3-fluoro-4-[[[3-hydroxy-5-(hydroxymethyl)-2-methyl-4-pyridinyl]methyl] amino]phenoxy]-, ethyl ester(926893-05-2)

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: 926893-05-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 926893-05-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,6,8,9 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 926893-05:
(8*9)+(7*2)+(6*6)+(5*8)+(4*9)+(3*3)+(2*0)+(1*5)=212
212 % 10 = 2
So 926893-05-2 is a valid CAS Registry Number.

926893-05-2Upstream product

926893-05-2Downstream Products

926893-05-2Relevant academic research and scientific papers

Structure-activity relationships of aryloxyalkanoic acid hydroxyamides as potent inhibitors of histone deacetylase

Marson, Charles M.,Mahadevan, Thevaki,Dines, Jon,Sengmany, Stephane,Morrell, James M.,Alao, John P.,Joel, Simon P.,Vigushin, David M.,Charles Coombes

, p. 136 - 141 (2007/10/03)

Syntheses of aryloxyalkanoic acid hydroxyamides are described, all of which are potent inhibitors of histone deacetylase, some being more potent in vitro than trichostatin A (IC50 = 3 nM). Variation of the substituents on the benzene ring as we

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