550809
Phenylguanidine carbonate salt
≥99%
Synonym(s):
1-Phenylguanidine carbonate, N-Phenylguanidine carbonate
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About This Item
Linear Formula:
C6H5NHC(=NH)NH2·(H2CO3)x
CAS Number:
Molecular Weight:
135.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
≥99%
Product Name
Phenylguanidine carbonate salt, ≥99%
InChI
1S/C7H9N3.CH2O3/c8-7(9)10-6-4-2-1-3-5-6;2-1(3)4/h1-5H,(H4,8,9,10);(H2,2,3,4)
SMILES string
OC(O)=O.NC(=N)Nc1ccccc1
InChI key
XDSYAIICRRZSJX-UHFFFAOYSA-N
assay
≥99%
mp
149-153 °C (lit.)
Quality Level
Application
Phenylguanidine carbonate salt may be used in the preparation of the following bioactive compounds:
- (E)-methyl 2-(2-((6-cyclopropyl-2-(phenylamino)pyrimidin-4-yloxy)methyl)phenyl)-3-methoxyacrylate
- cyprodinil
- 5,6-dihydropyrido[2,3-d]pyrimidine
- ethyl 1-methyl-8-(phenylamino)-4,5-dihydro-1H-pyrazolo[4,3-h]quinazoline-3-carboxylate
- 2-(phenylamino)-4-(trifluoromethyl)-1,6-dihydropyrimidine derivatives
Reactant involved in synthesis of polo-like kinase 1 inhibitors
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Synthesis of bactericide Cyprodinil.
Qu J, et al.
Zhejiang Gongye Daxue Xuebao (Journal of Zhejiang University of Technology), 1, 7-7 (2012)
Synthesis and SAR of new pyrazolo [4, 3-h] quinazoline-3-carboxamide derivatives as potent and selective MPS1 kinase inhibitors.
Caldarelli M, et al.
Bioorganic & Medicinal Chemistry Letters, 21(15), 4507-4511 (2011)
An unusual Michael addition of 3, 3-dimethoxypropanenitrile to 2-aryl acrylates: a convenient route to 4-unsubstituted 5, 6-dihydropyrido [2, 3-d] pyrimidines.
Berzosa X, et al.
The Journal of Organic Chemistry, 75(2), 487-490 (2009)
Synthesis of (E)-Methyl 2-(2-((6-cyclopropyl-2-(phenylamino) pyrimidin-4-yloxy) methyl) phenyl)-3-methoxyacrylate and Its Fungicidal Activity.
Li HC, et al.
Agrochemicals, 4, 6-6 (2009)
Solvent-Free Synthesis of 2-(Phenylamino)-4-(trifluoromethyl)-1, 6-dihydropyrimidine Derivatives Catalyzed by Sulfamic Acid.
Shen S, et al.
Journal of Heterocyclic Chemistry, 49(5), 1033-1037 (2012)
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