ChemicalBook--->CAS DataBase List--->2827-56-7

2827-56-7

2827-56-7 Structure

2827-56-7 Structure
IdentificationMore
[Name]

1-Aminohydantoin hydrochloride
[CAS]

2827-56-7
[Synonyms]

1-AMINO-2,4-IMIDAZOLIDINEDIONE HCL
1-AMINO-2,4-IMIDAZOLIDIONE HCL
1-AMINOHYDANTOIN HCL
1-AMINOHYDANTOIN HYDROCHLORIDE
1-AMINO-IMIDAZOLIDINE-2,4-DIONE HYDROCHLORIDE
TIMTEC-BB SBB004061
1-Amino-2,4-Imidazolinedione
1-Aminoimidazoline-2,4-dione hydrochloride
1-Aminohydantoin Hydrochloride, Vetranal
1-Aminohydantoine
1-AMINO-2,4-IMIDAZOLIDINEDIONE HYDROCHLORIDE
1-Amino-imidazolidine-2,4-dione Hydrochlorid
ahd
[Molecular Formula]

C3H6ClN3O2
[MDL Number]

MFCD02181047
[Molecular Weight]

151.55
[MOL File]

2827-56-7.mol
Chemical PropertiesBack Directory
[Appearance]

Pale Yellow Powder
[Melting point ]

201-205 °C(lit.)
[storage temp. ]

0-6°C
[solubility ]

DMSO (Slightly), Methanol (Slightly, Heated)
[form ]

Crystalline Powder
[color ]

Pale yellow
[biological source]

mouse
[BRN ]

3699376
[Stability:]

Unstable in Solution
[Major Application]

forensics and toxicology
pharmaceutical (small molecule)
[InChI]

1S/C3H5N3O2.ClH/c4-6-1-2(7)5-3(6)8;/h1,4H2,(H,5,7,8);1H
[InChIKey]

WEOHANUVLKERQI-UHFFFAOYSA-N
[SMILES]

Cl[H].NN1CC(=O)NC1=O
[CAS DataBase Reference]

2827-56-7(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319
[Precautionary statements ]

P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
[Hazard Codes ]

Xn
[Risk Statements ]

R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
[WGK Germany ]

3
[REACH Registrations]

Active
[HS Code ]

29332100
[Storage Class]

11 - Combustible Solids
Hazard InformationBack Directory
[Chemical Properties]

Pale Yellow Powder
[Uses]

A metabolite of Nitrofuran.
[Uses]

Reactant for synthesis of: Ectoparasiticidal drugs1 Skeletal muscle relaxants2Reactant for: Suzuki-Miyaura coupling3 Lymphoid specific tryosine phosphatase inhibitor4 Proteasome inhibition by peptide semicarbazones5
[Biological Activity]

Tumor Necrosis Factor (TNF)-Related Apoptosis-Inducing Ligand (TRAIL) activates the extrinsic apoptotic pathway by binding death receptors (DR) 4 and 5. In addition to DR 4 and 5TRAIL activates several other receptors such as decoy receptor (DcR)1DcR2 and a soluble receptor called osteoprotegerin. TRAIL plays a vital role in the inhibition of autoimmune inflammation and cell cycle progression. TRAIL selectively kills tumor cells without damaging normal tissues and thereforeit might act as a tumor-selective anticancer agent. TRAIL-induced apoptosis is involved in various cellular processes including activation-induced cell deathhomeostasisintrathymic negative selectionautoimmunity suppressionand immune surveillance. Repeated dosage of recombinant soluble TRAIL triggers apoptosisinhibits tumor progressionand increases viability of mice suffering from cancer.
Spectrum DetailBack Directory
[Spectrum Detail]

1-Aminohydantoin hydrochloride(2827-56-7)1HNMR
1-Aminohydantoin hydrochloride(2827-56-7)IR
Well-known Reagent Company Product InformationBack Directory
[Sigma Aldrich]

2827-56-7(sigmaaldrich)
[TCI AMERICA]

1-Aminohydantoin Hydrochloride,>98.0%(T)(2827-56-7)
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