Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
ClCO(CH2)6CO2CH3
CAS Number:
Molecular Weight:
206.67
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
96%
Form:
liquid
InChI
1S/C9H15ClO3/c1-13-9(12)7-5-3-2-4-6-8(10)11/h2-7H2,1H3
SMILES string
COC(=O)CCCCCCC(Cl)=O
InChI key
RKUPOLBFJIEWBZ-UHFFFAOYSA-N
assay
96%
form
liquid
refractive index
n20/D 1.45 (lit.)
density
1.456 g/mL at 25 °C (lit.)
functional group
acyl chloride, ester
Quality Level
Related Categories
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
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
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Synthesis and properties of PI polyamide?SAHA conjugate.
Ohtsuki et al.
Tetrahedron Letters, 50(52), 7288-7292 (2009)
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.
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 of 1-Aminocyclopropyl-Pentanoic and-Heptanoic Acid Derivatives.
Gensini et al.
Letters in Organic Chemistry, 5(5), 328-331 (2008)
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