141569
1-(4-Chlorophenyl)-1-cyclopentanecarboxylic acid
98%
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Assay
98%
form
solid
mp
162-164 °C (lit.)
SMILES string
OC(=O)C1(CCCC1)c2ccc(Cl)cc2
InChI
1S/C12H13ClO2/c13-10-5-3-9(4-6-10)12(11(14)15)7-1-2-8-12/h3-6H,1-2,7-8H2,(H,14,15)
InChI key
QJNFJEMGWIQMJT-UHFFFAOYSA-N
Biochem/physiol Actions
1-(4-Chlorophenyl)-1-cyclopentanecarboxylic acid reacts with diorganotin(IV) oxide or dichloride to yield organotin(IV) complexes having antitumor activities against various human cancer cell lines.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Inorganic chemistry, 50(17), 8158-8167 (2011-07-29)
The organotin(IV) compounds [Me(2)Sn(L)(2)] (1), [Et(2)Sn(L)(2)] (2), [(n)Bu(2)Sn(L)(2)] (3), [(n)Oct(2)Sn(L)(2)] (4), [Ph(2)Sn(L)(2)] (5), and [PhOSnL](6) (6) have been synthesized from the reactions of 1-(4-chlorophenyl)-1-cyclopentanecarboxylic acid (HL) with the corresponding diorganotin(IV) oxide or dichloride. They were characterized by IR and multinuclear
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