533653
5-Methylhydantoin
97%
Synonym(s):
5-Methyl-2,4-imidazolidinedione
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About This Item
Empirical Formula (Hill Notation):
C4H6N2O2
CAS Number:
Molecular Weight:
114.10
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
mp
148-152 °C (lit.)
SMILES string
CC1NC(=O)NC1=O
InChI
1S/C4H6N2O2/c1-2-3(7)6-4(8)5-2/h2H,1H3,(H2,5,6,7,8)
InChI key
VMAQYKGITHDWKL-UHFFFAOYSA-N
Application
Reactant for:
Preparation of N-chlorohydantoins
The Mitsunobu reaction
Pseudomonas putida strain allowing conversion into L-amino acids
D-hydantoinase from Agrobacteria tumefaceins
Eznymatic racemization
Preparation of N-chlorohydantoins
The Mitsunobu reaction
Pseudomonas putida strain allowing conversion into L-amino acids
D-hydantoinase from Agrobacteria tumefaceins
Eznymatic racemization
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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[Studies on the chemical constituents of Pueraria lobata].
M H Chen
Zhong yao tong bao (Beijing, China : 1981), 10(6), 34-36 (1985-06-01)
B A Nogueira et al.
The journal of physical chemistry. A, 124(31), 6303-6318 (2020-06-10)
The conformational space of 5-acetic acid hydantoin {5AAH; [2-(2,5-dioxoimidazolidin-4-yl)acetic acid]} was investigated by quantum chemical calculations performed at the DFT(B3LYP)/6-311++G(d,p) level of theory. A total of 13 conformers were located in the potential energy surface of the molecule, six of
M L Niku-Paavola et al.
Journal of applied microbiology, 86(1), 29-35 (1999-04-13)
New types of antimicrobial compounds were identified in the culture filtrate of Lactobacillus plantarum VTT E-78076. Activity was detected in the low molecular mass fraction separated by gel chromatography. This fraction totally inhibited the growth of the Gram-negative test organism
C L Soong et al.
FEMS microbiology letters, 158(1), 51-55 (1998-02-07)
Cyclic imide-transforming activity was found to be widely distributed in bacteria, yeast and molds. This activity was not correlated with cyclic ureide-transforming activity in bacteria, but there was some correlation in yeast and molds. These two activities are probably catalyzed
Anupama S Engineer et al.
Enzyme and microbial technology, 138, 109554-109554 (2020-06-13)
Overexpression of a novel hydantoinase (hyuH) from P. aeruginosa (MCM B-887) in E. coli yielded optically pure carbamoyl amino acids. The use of optically pure carbamoyl amino acids as substrates facilitates the synthesis of non-proteinogenic amino acids. The enzyme hyuH
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