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MedKoo Cat#: 591839 | Name: Phenyl 2-thienyl ketone

Description:

WARNING: This product is for research use only, not for human or veterinary use.

Phenyl 2-thienyl ketone is a biochemical.

Chemical Structure

Phenyl 2-thienyl ketone
Phenyl 2-thienyl ketone
CAS#135-00-2

Theoretical Analysis

MedKoo Cat#: 591839

Name: Phenyl 2-thienyl ketone

CAS#: 135-00-2

Chemical Formula: C11H8OS

Exact Mass: 188.0296

Molecular Weight: 188.24

Elemental Analysis: C, 70.19; H, 4.28; O, 8.50; S, 17.03

Price and Availability

Size Price Availability Quantity
5g USD 220.00
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Related CAS #
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Synonym
Phenyl 2-thienyl ketone; AI3-11217; AI3 11217; AI311217
IUPAC/Chemical Name
Methanone, phenyl-2-thienyl-
InChi Key
DWYFUJJWTRPARQ-UHFFFAOYSA-N
InChi Code
InChI=1S/C11H8OS/c12-11(10-7-4-8-13-10)9-5-2-1-3-6-9/h1-8H
SMILES Code
O=C(C1=CC=CC=C1)C2=CC=CS2
Appearance
Solid powder
Purity
>98% (or refer to the Certificate of Analysis)
Shipping Condition
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Storage Condition
Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).
Solubility
Soluble in DMSO
Shelf Life
>3 years if stored properly
Drug Formulation
This drug may be formulated in DMSO
Stock Solution Storage
0 - 4 C for short term (days to weeks), or -20 C for long term (months).
HS Tariff Code
2934.99.03.00
More Info

Preparing Stock Solutions

The following data is based on the product molecular weight 188.24 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
1: Gedik Z, Tugrak M, Dastan A, Gul HI, Yilmaz D. Radiation Parameters of Some Potential Bioactive Compounds. Guang Pu Xue Yu Guang Pu Fen Xi. 2015 Jun;35(6):1501-5. PubMed PMID: 26601355. 2: Bekhit AA, Haimanot T, Hymete A. Evaluation of some 1H-pyrazole derivatives as a dual acting antimalarial and anti-leishmanial agents. Pak J Pharm Sci. 2014 Nov;27(6):1767-73. PubMed PMID: 25362601. 3: Canturk P, Kucukoglu K, Topcu Z, Gul M, Gul HI. Effect of some bis Mannich bases and corresponding piperidinols on DNA topoisomerase I. Arzneimittelforschung. 2008;58(12):686-91. PubMed PMID: 19202742. 4: Gul HI, Cizmecioglu M, Zencir S, Gul M, Canturk P, Atalay M, Topcu Z. Cytotoxic activity of 4'-hydroxychalcone derivatives against Jurkat cells and their effects on mammalian DNA topoisomerase I. J Enzyme Inhib Med Chem. 2009 Jun;24(3):804-7. doi: 10.1080/14756360802399126. PubMed PMID: 18830876. 5: Gul HI, Calls U, Ozturk Z, Tutar E, Calikiran L. Evaluation of anticonvulsant activities of bis(3-aryl-3-oxo-propyl) ethylamine hydrochlorides and 4-aryl-3-arylcarbonyl-1-ethyl-4-piperidinol hydrochlorides. Arzneimittelforschung. 2007;57(3):133-6. PubMed PMID: 17469646. 6: Gul HI, Sahin F, Gul M, Ozturk S, Yerdelen KO. Evaluation of antimicrobial activities of several mannich bases and their derivatives. Arch Pharm (Weinheim). 2005 Jul;338(7):335-8. PubMed PMID: 15981301. 7: Gul HI, Gul M, Erciyas E. Toxicity of some bis Mannich bases and corresponding piperidinols in the brine shrimp (Artemia salina) bioassay. J Appl Toxicol. 2003 Jan-Feb;23(1):53-7. PubMed PMID: 12518337. 8: Nabana T, Togo H. Reactivities of novel [hydroxy(tosyloxy)iodo]arenes and [hydroxy(phosphoryloxy)iodo]arenes for alpha-tosyloxylation and alpha-phosphoryloxylation of ketones. J Org Chem. 2002 Jun 14;67(12):4362-5. PubMed PMID: 12054975. 9: Baumgartner MT, Gallego MH, Pierini AB. Synthesis of 2-Phenyl-1-(2-thienyl)- and 2-Aryl-1-(2-furyl)ethanones by the S(RN)1 Mechanism. Relative Reactivities of Enolate Ions of Ketones. J Org Chem. 1998 Sep 4;63(18):6394-6397. PubMed PMID: 11672276. 10: Hsu LY, Lee CF, Chou TC, Ding YA. 2-Heteroaryl 2-substituted phenylketone derivatives and their inhibitory activity on platelet aggregation. J Pharm Pharmacol. 1995 Sep;47(9):762-7. PubMed PMID: 8583390. 11: De Guidi G, Chillemi R, Costanzo LL, Giuffrida S, Sortino S, Condorelli G. Molecular mechanism of drug photosensitization. 5. Photohemolysis sensitized by Suprofen. J Photochem Photobiol B. 1994 May;23(2-3):125-33. PubMed PMID: 8040753. 12: Massa S, Di Santo R, Costi R, Simonetti G, Retico A, Apuzzo G, Artico M. Antifungal agents. III. Naphthyl and thienyl derivatives of 1H-imidazol-1-yl-4-phenyl-1H-pyrrol-3-ylmethane. Farmaco. 1993 Jun;48(6):725-36. PubMed PMID: 8373500. 13: Wascher TC, Dittrich P, Kukovetz WR. LG 6-101 and LG 6-102, two new propafenone-related antiarrhythmic agents with good oral activity in rats. Naunyn Schmiedebergs Arch Pharmacol. 1992 Apr;345(4):473-7. PubMed PMID: 1620247. 14: Wascher TC, Dittrich P, Kukovetz WR. Antiarrhythmic effects of two new propafenone related drugs. A study on four animal models of arrhythmia. Arzneimittelforschung. 1991 Feb;41(2):119-24. PubMed PMID: 2043172. 15: Reid AA, Kim CH, Thurkauf A, Monn JA, de Costa B, Jacobson AE, Rice KC, Bowen WD, Rothman RB. Wash-resistant inhibition of phencyclidine- and haloperidol-sensitive sigma receptor sites in guinea pig brain by putative affinity ligands: determination of selectivity. Neuropharmacology. 1990 Nov;29(11):1047-53. PubMed PMID: 1965013. 16: de Costa BR, George C, Burke TR Jr, Rafferty MF, Contreras PC, Mick SJ, Jacobson AE, Rice KC. Synthesis, configuration, and evaluation of two conformationally restrained analogues of phencyclidine. J Med Chem. 1988 Aug;31(8):1571-5. PubMed PMID: 3397994.