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4,7-Dimethyl-1,10-phenanthroline - 98%, high purity , CAS No.3248-05-3

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4,7-Dimethyl-1,10-phenanthroline - 98%, high purity , CAS No.3248-05-3

1 Citations

COA

Grade & Purity:

≥98%

Cas Number: 3248-05-3
Molecular Weight: 208.26
EC Number: 221-827-5
MDL number: MFCD00004979
PubChem CID: 72792
PubChem SID: 488184713

In stock

Item Number

D119916

Grouped product items
SKU	Size	Availability	Price
D119916-250mg	250mg	3	$86.90
D119916-1g	1g	3	$206.90
D119916-5g	5g	3	$824.90

View related series

Halogen free heterocyclic block (1207) Nitrogen donating ligand (229)

Basic Description

Synonyms	5-Fluoro-l-(2-furanidinyl)-4-(trimethylsilyloxy)-2-pyrimidone \| P3YJ54Z8ZO \| SCHEMBL182930 \| DS-2431 \| DTXSID9062932 \| NSC 4281 \| 4,7-Dimethyl-(1,10)phenanthroline \| Nitrotetrazolium Blue \| UNII-P3YJ54Z8ZO \| AKOS003369115 \| EINECS 221-827-5 \| PD007843 \| M
Specifications & Purity	≥98%
Shipped In	Normal
Product Description	application： 4,7-Dimethyl-1,10-phenanthroline acts as an intermediate in synthetic chemistry and dyestuff field. It is also used as an organic bidentate ligand and form complexes with metal for detection. Further, it plays an important role in colorimetric sensors, coordination polymer, ionochromism and luminescence.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Class Phenanthrolines

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Class	Phenanthrolines
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Phenanthrolines
Alternative Parents	Quinolines and derivatives Methylpyridines Benzenoids Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
Molecular Framework	Aromatic heteropolycyclic compounds
Substituents	1,10-phenanthroline - Quinoline - Methylpyridine - Benzenoid - Pyridine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as phenanthrolines. These are aromatic polycyclic compounds containing the phenanthroline skeleton, which is a derivative of phenanthrene, and consists of two pyridine rings non-linearly joined by a benzene ring.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Associated Targets(Human)

CCR1 Tchem C-C chemokine receptor type 1 (1730 Activities)

Discover Target: CCR1

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

CCR5 Tclin C-C chemokine receptor type 5 (5640 Activities)

Discover Target: CCR5

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mechanisms of Action

Mechanism of Action	Action Type	target ID	Target Name	Target Type	Target Organism	Binding Site Name	References

Names and Identifiers

Pubchem Sid	488184713
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488184713
IUPAC Name	4,7-dimethyl-1,10-phenanthroline
INCHI	InChI=1S/C14H12N2/c1-9-5-7-15-13-11(9)3-4-12-10(2)6-8-16-14(12)13/h3-8H,1-2H3
InChIKey	JIVLDFFWTQYGSR-UHFFFAOYSA-N
Smiles	CC1=C2C=CC3=C(C=CN=C3C2=NC=C1)C
Isomeric SMILES	CC1=C2C=CC3=C(C=CN=C3C2=NC=C1)C
Molecular Weight	208.26
Reaxy-Rn	154062
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=154062&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

11 results found

Lot Number	Certificate Type	Date	Item
A1323045	Certificate of Analysis	Nov 04, 2024	D119916
I2413330	Certificate of Analysis	Apr 11, 2024	D119916
B2505139	Certificate of Analysis	Apr 11, 2024	D119916
G2404575	Certificate of Analysis	Apr 11, 2024	D119916
G2404577	Certificate of Analysis	Apr 11, 2024	D119916
H2206846	Certificate of Analysis	Jun 23, 2022	D119916
G2312102	Certificate of Analysis	Jun 23, 2022	D119916
H2206620	Certificate of Analysis	Jun 23, 2022	D119916
F2316933	Certificate of Analysis	Jun 23, 2022	D119916
H2206619	Certificate of Analysis	Jun 23, 2022	D119916
F2316932	Certificate of Analysis	Nov 23, 2021	D119916

Show more⌵

Chemical and Physical Properties

Solubility	Soluble in benzene and alcohol. Slightly soluble in water.
Melt Point(°C)	190-196°C
Molecular Weight	208.260 g/mol
XLogP3	3.200
Hydrogen Bond Donor Count	0
Hydrogen Bond Acceptor Count	2
Rotatable Bond Count	0
Exact Mass	208.1 Da
Monoisotopic Mass	208.1 Da
Topological Polar Surface Area	25.800 Å²
Heavy Atom Count	16
Formal Charge	0
Complexity	227.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

Citations of This Product

How to Cite Aladdin Scientific Products?

1. H. C. Guo, R. H. Zheng, H. J. Jiang. (2012) Improved Synthesis of 2,9-Dichloro-1,10-phenanthroline. ORGANIC PREPARATIONS AND PROCEDURES INTERNATIONAL,

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