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385565

Sigma-Aldrich

Methyl 8-chloro-8-oxooctanoate

96%

Synonym(s):

Methyl suberyl chloride

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About This Item

Linear Formula:
ClCO(CH2)6CO2CH3
CAS Number:
Molecular Weight:
206.67
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

96%

form

liquid

refractive index

n20/D 1.45 (lit.)

density

1.456 g/mL at 25 °C (lit.)

SMILES string

COC(=O)CCCCCCC(Cl)=O

InChI

1S/C9H15ClO3/c1-13-9(12)7-5-3-2-4-6-8(10)11/h2-7H2,1H3

InChI key

RKUPOLBFJIEWBZ-UHFFFAOYSA-N

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


Certificates of Analysis (COA)

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A cyclodextrin-capped histone deacetylase inhibitor.
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A fluorescent assay for the evaluation of inhibitors of fatty acid amide hydrolase (FAAH) is described. Microsomes from rat brain served as enzyme source. N-(2-Hydroxyethyl)-4-pyren-1-ylbutanamide was designed and synthesized as novel fluorogenic substrate. For substrate solubilization, Triton X-100 was employed.
Synthesis of 1-Aminocyclopropyl-Pentanoic and-Heptanoic Acid Derivatives.
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Letters in Organic Chemistry, 5(5), 328-331 (2008)
Synthesis and properties of PI polyamide?SAHA conjugate.
Ohtsuki et al.
Tetrahedron Letters, 50(52), 7288-7292 (2009)
John Spencer et al.
ACS medicinal chemistry letters, 2(5), 358-362 (2011-05-17)
N(1)-Hydroxy-N(8)-ferrocenyloctanediamide, JAHA (7), an organometallic analogue of SAHA containing a ferrocenyl group as a phenyl bioisostere, displays nanomolar inhibition of class I HDACs, excellent selectivity over class IIa HDACs, and anticancer action in intact cells (IC(50) = 2.4 μM, MCF7

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