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About This Item
Empirical Formula (Hill Notation):
C4H6N2O2
CAS Number:
Molecular Weight:
114.10
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
97%
Quality Level
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
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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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
[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)
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 533653-1G | 04061826706145 |
