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N-Phenylacrylamide - >98.0%(GC), high purity , CAS No.2210-24-4

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N-Phenylacrylamide - >98.0%(GC), high purity , CAS No.2210-24-4

1 Citations

COA

Grade & Purity:

≥98%(GC)

Cas Number: 2210-24-4
Molecular Weight: 147.18
MDL number: MFCD00080617
PubChem CID: 221792
PubChem SID: 488188693

In stock

Item Number

N159041

Grouped product items
SKU	Size	Availability	Price
N159041-250mg	250mg	3	$9.90
N159041-1g	1g	4	$26.90
N159041-5g	5g	9	$103.90
N159041-25g	25g	2	$364.90
N159041-100g	100g	1	$1,313.90

View related series

Acrylic monomer (124) Anti-infection (2803) Fungal (844) Polymer / polymer reagent (675)

Basic Description

Synonyms	CS-W019368 \| Asylanilide \| DS-6577 \| HY-W018582 \| SCHEMBL81209 \| N-Phenylacrylateamide \| N-Phenylacrylamide, 99% \| Z440633536 \| N1-Phenylacrylamide \| N-PHENYL-2-PROPENAMIDE \| NSC 6857 \| SCHEMBL13341546 \| n-acryloylaniline \| UNII-A2AQJ9FV2G \| AMY19693 \| AQ
Specifications & Purity	≥98%(GC)
Shipped In	Normal

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Benzenoids
  - Class Benzene and substituted derivatives
    - Subclass Anilides

Kingdom	Organic compounds
Superclass	Benzenoids
Class	Benzene and substituted derivatives
Subclass	Anilides
Intermediate Tree Nodes	Not available
Direct Parent	Anilides
Alternative Parents	N-arylamides Acrylic acids and derivatives Secondary carboxylic acid amides Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Anilide - N-arylamide - Acrylic acid or derivatives - Secondary carboxylic acid amide - Carboxamide group - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aromatic homomonocyclic compound
Description	This compound belongs to the class of organic compounds known as anilides. These are organic heterocyclic compounds derived from oxoacids RkE(=O)l(OH)m (l not 0) by replacing an OH group by the NHPh group or derivative formed by ring substitution.
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)

F2 Tclin Thrombin (11687 Activities)

Discover Target: F2

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

METAP1 Tchem Methionine aminopeptidase 1 (614 Activities)

Discover Target: METAP1

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

FBP1 Tchem Fructose-1,6-bisphosphatase (1199 Activities)

Discover Target: FBP1

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

TGM2 Tchem Protein-glutamine gamma-glutamyltransferase (1221 Activities)

Discover Target: TGM2

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

HeLa (62764 Activities)

Explore this target

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	488188693
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488188693
IUPAC Name	N-phenylprop-2-enamide
INCHI	InChI=1S/C9H9NO/c1-2-9(11)10-8-6-4-3-5-7-8/h2-7H,1H2,(H,10,11)
InChIKey	BPCNEKWROYSOLT-UHFFFAOYSA-N
Smiles	C=CC(=O)NC1=CC=CC=C1
Isomeric SMILES	C=CC(=O)NC1=CC=CC=C1
Molecular Weight	147.18
Reaxy-Rn	2078220
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2078220&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.

9 results found

Lot Number	Certificate Type	Date	Item
D1925093	Certificate of Analysis	Feb 06, 2023	N159041
K2315109	Certificate of Analysis	Feb 06, 2023	N159041
L2220039	Certificate of Analysis	Jan 05, 2023	N159041
G2207433	Certificate of Analysis	Jun 08, 2022	N159041
G2207435	Certificate of Analysis	Jun 08, 2022	N159041
G2207434	Certificate of Analysis	Jun 08, 2022	N159041
G2207432	Certificate of Analysis	Jun 08, 2022	N159041
G2207430	Certificate of Analysis	Jun 08, 2022	N159041
B2215172	Certificate of Analysis	Feb 18, 2022	N159041

Chemical and Physical Properties

Melt Point(°C)	105℃
Molecular Weight	147.170 g/mol
XLogP3	1.800
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	2
Exact Mass	147.068 Da
Monoisotopic Mass	147.068 Da
Topological Polar Surface Area	29.100 Å²
Heavy Atom Count	11
Formal Charge	0
Complexity	148.000
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. Saifei Fang, Xin Pu, Ali Usman, Jiawen Hu, Xin Han, Lei Ye, Yunlong Qin, Pengpeng Liu, Bo Luan, Jichang Liu. (2024) Performance improvement on the cold flow properties of crude oil with high asphaltene by adjusting the polarity of the third monomer in polymers. JOURNAL OF APPLIED POLYMER SCIENCE, 141 (16): (e55254).

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