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Formanilide - 99%, high purity , CAS No.103-70-8

2 Citations

COA

Grade & Purity:

≥99%

Cas Number: 103-70-8
Molecular Weight: 121.14
Beilstein Registry Number: 12230
EC Number: MFCD00003276
MDL number: MFCD00003276
PubChem CID: 7671
PubChem SID: 488180521

In stock

Item Number

F112354

Grouped product items
SKU	Size	Availability	Price
F112354-5g	5g	6	$9.90
F112354-25g	25g	5	$15.90
F112354-100g	100g	5	$42.90
F112354-500g	500g	1	$192.90

View related series

amide (313) Non heterocyclic block (8163)

Basic Description

Synonyms	DTXSID3025338 \| CAS-103-70-8 \| N-Formylaniline \| N-Formyl-aniline \| SCHEMBL2463 \| AI3-01089 \| MLS002415732 \| Q2689660 \| Tox21_200271 \| BIDD:GT0244 \| F0047 \| NCGC00091354-01 \| SMR001370900 \| FT-0626529 \| N-Formanilide \| formanilid \| Formanilide \| FORMANILI
Specifications & Purity	≥99%
Storage Temp	Store at 2-8°C
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.

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 Secondary carboxylic acid amides Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aromatic homomonocyclic compounds
Substituents	Anilide - N-arylamide - 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	formamides - aromatic amide
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)

ALDH1A1 Tchem Aldehyde dehydrogenase 1A1 (77053 Activities)

Discover Target: ALDH1A1

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

SMAD3 Tchem Mothers against decapentaplegic homolog 3 (68039 Activities)

Discover Target: SMAD3

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

GMNN Tbio Geminin (128009 Activities)

Discover Target: GMNN

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

Associated Targets(non-human)

Ppard Peroxisome proliferator-activated receptor delta (358 Activities)

Discover Target: Ppard

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

Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)

Discover Target: Nfe2l2

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	488180521
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488180521
IUPAC Name	N-phenylformamide
INCHI	InChI=1S/C7H7NO/c9-6-8-7-4-2-1-3-5-7/h1-6H,(H,8,9)
InChIKey	DYDNPESBYVVLBO-UHFFFAOYSA-N
Smiles	C1=CC=C(C=C1)NC=O
Isomeric SMILES	C1=CC=C(C=C1)NC=O
WGK Germany	2
RTECS	BY1780000
Molecular Weight	121.14
Beilstein	12230
Reaxy-Rn	906934
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=906934&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
C1717028	Certificate of Analysis	Nov 01, 2024	F112354
D2419058	Certificate of Analysis	Apr 19, 2023	F112354
E2326481	Certificate of Analysis	Apr 19, 2023	F112354
E2326538	Certificate of Analysis	Apr 19, 2023	F112354
E2326473	Certificate of Analysis	Apr 19, 2023	F112354
E2326472	Certificate of Analysis	Apr 19, 2023	F112354
E2326486	Certificate of Analysis	Apr 19, 2023	F112354
E2326535	Certificate of Analysis	Apr 19, 2023	F112354
E2326482	Certificate of Analysis	Apr 19, 2023	F112354
E2508064	Certificate of Analysis	Apr 19, 2023	F112354
B2310621	Certificate of Analysis	Feb 17, 2023	F112354

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Chemical and Physical Properties

Refractive Index	1.578
Flash Point(°F)	235.4 °F
Flash Point(°C)	113 °C
Boil Point(°C)	271°C
Melt Point(°C)	46-48°C
Molecular Weight	121.140 g/mol
XLogP3	1.200
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	1
Exact Mass	121.053 Da
Monoisotopic Mass	121.053 Da
Topological Polar Surface Area	29.100 Å²
Heavy Atom Count	9
Formal Charge	0
Complexity	86.900
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. Congcong Chen, Zhiqiang Xu, Jiemin Qiu, Weihao Ye, Xiaokai Xu, Ruizhe Wang, Chaofan Hu, Jianle Zhuang, Bingfu Lei, Wei Li, Xuejie Zhang, Guangqi Hu, Yingliang Liu. (2022) Synthesis of Carbon Dots with Carbogenic π-Conjugated Domains for Full-Band UV Shielding. ACS Applied Nano Materials, 5 (7): (9140–9149).
2. Xiaomeng Deng, Wensheng Wei, Zizhen Yan, Zhanguo Zhang, Yuxin Wang, Guangwen Xu, Jianjun Guo, Jinggang Zhao, Lei Shi. (2024) Product as additive for facilitating CO2 conversion into cyclic carbonate. Journal of CO2 Utilization, 84 (102850).

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