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1-Adamantylthiourea - 97%, high purity , CAS No.25444-82-0

COA

Grade & Purity:

≥97%

Cas Number: 25444-82-0
Molecular Weight: 210.34
PubChem CID: 796429

In stock

Item Number

A151182

Grouped product items
SKU	Size	Availability	Price
A151182-250mg	250mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$20.90
A151182-1g	1g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$55.90
A151182-5g	5g	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$196.90

Basic Description

Synonyms	1-Adamantylthiourea \| 25444-82-0 \| N-1-adamantylthiourea \| 1-(Adamantan-1-yl)thiourea \| (adamantan-1-yl)thiourea \| 1-(1-Adamantyl)thiourea \| adamantylthiourea \| N1-Adamantylthiourea \| NSC184815 \| 1-((3s,5s,7s)-adamantan-1-yl)thiourea \| CBMicro_020308 \| Thiourea, adamantan-1-yl
Specifications & Purity	≥97%
Shipped In	Normal
Product Description	Product Application： 1-Adamantylthiourea performs a viral inhibitory activity against influenza virus A2 infections in mice.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organosulfur compounds
  - Class Thioureas

Kingdom	Organic compounds
Superclass	Organosulfur compounds
Class	Thioureas
Subclass	Not available
Intermediate Tree Nodes	Not available
Direct Parent	Thioureas
Alternative Parents	Organopnictogen compounds Organonitrogen compounds Hydrocarbon derivatives
Molecular Framework	Aliphatic homopolycyclic compounds
Substituents	Thiourea - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Aliphatic homopolycyclic compound
Description	This compound belongs to the class of organic compounds known as thioureas. These are organic compounds containing the thiourea functional group, a derivative of urea with the general structure (R1(N)R2C(=S)(R3)R4, R1-R4=H, alkyl, aryl), obtained by replacing the carbonyl group of urea with a thiocarbonyl group.
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

Mechanisms of Action

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

Names and Identifiers

IUPAC Name	1-adamantylthiourea
INCHI	InChI=1S/C11H18N2S/c12-10(14)13-11-4-7-1-8(5-11)3-9(2-7)6-11/h7-9H,1-6H2,(H3,12,13,14)
InChIKey	LRWQENBAFMBIJR-UHFFFAOYSA-N
Smiles	C1C2CC3CC1CC(C2)(C3)NC(=S)N
Isomeric SMILES	C1C2CC3CC1CC(C2)(C3)NC(=S)N
Molecular Weight	210.34
Reaxy-Rn	2211902
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2211902&ln=

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

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Analytical Chart:

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Lot Number	Certificate Type	Date	Item
H2402110	Certificate of Analysis	Apr 16, 2024	A151182

Chemical and Physical Properties

Molecular Weight	210.340 g/mol
XLogP3	2.300
Hydrogen Bond Donor Count	2
Hydrogen Bond Acceptor Count	1
Rotatable Bond Count	1
Exact Mass	210.119 Da
Monoisotopic Mass	210.119 Da
Topological Polar Surface Area	70.100 Å²
Heavy Atom Count	14
Formal Charge	0
Complexity	233.000
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

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