Skip to Content
Merck
All Photos(1)

Key Documents

View All Documentation

385565

Sigma-Aldrich

Methyl 8-chloro-8-oxooctanoate

96%

Synonym(s):

Methyl suberyl chloride

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
ClCO(CH2)6CO2CH3
CAS Number:
41624-92-4
Molecular Weight:
206.67
MDL number:
MFCD00134649
UNSPSC Code:
12352100
PubChem Substance ID:
24864038
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
GHS05

Signal Word

Danger

Hazard Statements

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

A cyclodextrin-capped histone deacetylase inhibitor.
Amin et al.
Biochemical Medicine, 23(11), 3346-3348 (2013)
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
Synthesis and properties of PI polyamide?SAHA conjugate.
Ohtsuki et al.
Tetrahedron Letters, 50(52), 7288-7292 (2009)
Synthesis of 1-Aminocyclopropyl-Pentanoic and-Heptanoic Acid Derivatives.
Gensini et al.
Letters in Organic Chemistry, 5(5), 328-331 (2008)
Laura Forster et al.
Analytical and bioanalytical chemistry, 394(6), 1679-1685 (2009-06-02)
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.
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service