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N-(2-Fluorenyl)acetamide - 98%, high purity , CAS No.53-96-3

  • ≥98%
Item Number
F106909
Grouped product items
SKUSizeAvailabilityPrice Qty
F106909-250mg
250mg
In stock
$9.90
F106909-1g
1g
In stock
$20.90
F106909-5g
5g
In stock
$79.90
F106909-25g
25g
In stock
$231.90
View related series
Carbonyl compound Cyclopentadiene

Basic Description

Synonyms2-Acetamidofluorene|2-Acetylaminofluorene|53-96-3|N-(9H-Fluoren-2-yl)acetamide|N-2-Fluorenylacetamide|2-AAF|N-acetyl-2-aminofluorene|Acetamide, N-9H-fluoren-2-yl-|2-(Acetylamino)fluorene|2-FAA|N-Fluoren-2-ylacetamide|2-Acetaminofluorene|2-Fluorenylacetami
Specifications & Purity≥98%
Biochemical and Physiological MechanismsA genotoxic carcinogen that is used to model liver carcinogenesis in rat. When N-hydroxylated by cytochrome CYP1A2 in the liver, 2-AAF forms adducts with DNA and is tumorigenic in liver and bladder.
Storage TempProtected from light,Argon charged
Shipped InNormal
Product Description

Usually used to induce liver cancer in animal models such as the 2-AAF/partial hepatectomy rat, study the mechanism of liver carcinogenesis and as a reference material during its identification or quantitation.

Associated Targets

CTH Tchem Cystathionine gamma-lyase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP1A2 Tchem Cytochrome P450 1A2 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CNR1 Tclin Cannabinoid receptor 1 0 Activities

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DRD2 Tclin D(2) dopamine receptor 0 Activities

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DRD4 Tchem D(4) dopamine receptor 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

CYP3A4 Tclin Cytochrome P450 3A4 0 Activities

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ERBB2 Tclin Receptor tyrosine-protein kinase erbB-2 0 Activities

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ELANE Tclin Neutrophil elastase 0 Activities

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EGFR Tclin Epidermal growth factor receptor 0 Activities

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AVPR1A Tclin Vasopressin V1a receptor 0 Activities

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ABCB1 Tchem Multidrug resistance protein 1 0 Activities

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HMGCR Tclin 3-hydroxy-3-methylglutaryl-coenzyme A reductase 0 Activities

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HRH1 Tclin Histamine H1 receptor 0 Activities

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SLC6A3 Tclin Sodium-dependent dopamine transporter 0 Activities

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SLC6A4 Tclin Sodium-dependent serotonin transporter 0 Activities

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SIGMAR1 Tclin Sigma non-opioid intracellular receptor 1 0 Activities

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PTGS1 Tclin Prostaglandin G/H synthase 1 0 Activities

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CA2 Tclin Carbonic anhydrase 2 0 Activities

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DRD3 Tclin D(3) dopamine receptor 0 Activities

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FLT1 Tclin Vascular endothelial growth factor receptor 1 0 Activities

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CHRM3 Tclin Muscarinic acetylcholine receptor M3 0 Activities

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CHRM4 Tclin Muscarinic acetylcholine receptor M4 0 Activities

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ADRA2B Tclin Alpha-2B adrenergic receptor 0 Activities

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ADRA2C Tclin Alpha-2C adrenergic receptor 0 Activities

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HTR2A Tclin 5-hydroxytryptamine receptor 2A 0 Activities

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ADORA2A Tclin Adenosine receptor A2a 0 Activities

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ACHE Tclin Acetylcholinesterase 0 Activities

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ADRA1B Tclin Alpha-1B adrenergic receptor 0 Activities

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ADRA2A Tclin Alpha-2A adrenergic receptor 0 Activities

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ADRB1 Tclin Beta-1 adrenergic receptor 0 Activities

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ADRA1A Tclin Alpha-1A adrenergic receptor 0 Activities

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AR Tclin Androgen receptor 0 Activities

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MAOA Tclin Amine oxidase [flavin-containing] A 1 Activities

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AKR1B1 Tclin Aldose reductase 0 Activities

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ADORA1 Tclin Adenosine receptor A1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HTR1A Tclin 5-hydroxytryptamine receptor 1A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ADORA3 Tchem Adenosine receptor A3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HTR6 Tchem 5-hydroxytryptamine receptor 6 0 Activities

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HTR2B Tclin 5-hydroxytryptamine receptor 2B 0 Activities

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EDNRA Tclin Endothelin-1 receptor 0 Activities

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KCNH2 Tclin Potassium voltage-gated channel subfamily H member 2 0 Activities

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OPRD1 Tclin Delta-type opioid receptor 0 Activities

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OPRK1 Tclin Kappa-type opioid receptor 0 Activities

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OPRM1 Tclin Mu-type opioid receptor 0 Activities

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NOS2 Tchem Nitric oxide synthase, inducible 0 Activities

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TACR1 Tclin Substance-P receptor 0 Activities

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NOS1 Tchem Nitric oxide synthase, brain 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

Pubchem Sid488179955
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488179955
IUPAC Name N-(9H-fluoren-2-yl)acetamide
INCHI InChI=1S/C15H13NO/c1-10(17)16-13-6-7-15-12(9-13)8-11-4-2-3-5-14(11)15/h2-7,9H,8H2,1H3,(H,16,17)
InChi Key CZIHNRWJTSTCEX-UHFFFAOYSA-N
Canonical SMILES CC(=O)NC1=CC2=C(C=C1)C3=CC=CC=C3C2
Isomeric SMILES CC(=O)NC1=CC2=C(C=C1)C3=CC=CC=C3C2
WGK Germany 3
RTECS AB9450000
PubChem CID 5897
UN Number 3077
Packing Group III
Molecular Weight 223.27
Beilstein 2807677
Reaxy-Rn 2807677

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

To view the certificate results,please click on a Lot number.For Lot numbers from past orders,please use our order status section

8 results found

Lot NumberCertificate TypeDateItem
G2307213Certificate of AnalysisMay 12, 2023 F106909
G2307245Certificate of AnalysisMay 12, 2023 F106909
G2307282Certificate of AnalysisMay 12, 2023 F106909
G2307283Certificate of AnalysisMay 12, 2023 F106909
G2307284Certificate of AnalysisMay 12, 2023 F106909
G2307286Certificate of AnalysisMay 12, 2023 F106909
G2307302Certificate of AnalysisMay 12, 2023 F106909
G2307314Certificate of AnalysisMay 12, 2023 F106909

Chemical and Physical Properties

SolubilityInsoluble in water; Soluble in Alcohol,Ether
SensitivityLight & Moisture Sensitive
Melt Point(°C)192-196°C

Safety and Hazards(GHS)

Pictogram(s) GHS08,   GHS07
Signal Danger
Hazard Statements

H302:Harmful if swallowed

H350:May cause cancer

Precautionary Statements

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P405:Store locked up.

P501:Dispose of contents/container to ...

P264:Wash hands [and …] thoroughly after handling.

P270:Do not eat, drink or smoke when using this product.

P330:Rinse mouth.

P203:Obtain, read and follow all safety instructions before use.

P301+P317:IF SWALLOWED: Get medical help.

P318:if exposed or concerned, get medical advice.

WGK Germany 3
RTECS AB9450000
Reaxy-Rn 2807677
Class 9
Merck Index 4157

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