126-06-7|3-Bromo-1-chloro-5,5-dimethylhydantoin

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3-Bromo-1-chloro-5,5-dimethylhydantoin | CAS:126-06-7

3-Bromo-1-chloro-5,5-dimethylhydantoin

Name：3-Bromo-1-chloro-5,5-dimethylhydantoin
CAS：126-06-7
Synonyms：BCDMH; 3-Bromo-1-chloro-5,5-dimethyl-2,4-imidazolinedione
Molecular Formula：C₅H₆BrClN₂O₂
Molecular Weight：241.47
EINESC：204-766-9

Description

Properties

Melting point	159-163 ºC

Safety

Symbol(GHS)	O;C
Hazard Codes	R8;R31;R34
SDS/MSDS	S8;S17;S26;S36/37/39;S41;S45

SDS

Source	SDS/MSDS Samples
没有数据	没有数据

Synthetic Route

Name	CAS

Articles

Peer-Reviewed Papers

Biotransformation of anthocyanins from Vitis amurensis Rupr of "Beibinghong" extract by human intestinal microbiota.Fei Zheng et al.Xenobiotica; the fate of foreign compounds in biological systems, 49(9), 1025-1032 (2018-10-24) Discovery of protein disulfide isomerase P5 inhibitors that reduce the secretion of MICA from cancer cells.Tomohisa Horibe et al.Chembiochem : a European journal of chemical biology, 15(11), 1599-1606 (2014-06-13) Hemidesmus indicus (L.) R. Br. extract inhibits the early step of herpes simplex type 1 and type 2 replication.Francesca Bonvicini et al.The new microbiologica, 41(3), 187-194 (2018-06-07) Testing the Pharmacokinetic Interactions of 24 Colonic Flavonoid Metabolites with Human Serum Albumin and Cytochrome P450 Enzymes.Violetta Mohos et al.Biomolecules, 10(3) (2020-03-12) Inhibitory Effects of Quercetin and Its Human and Microbial Metabolites on Xanthine Oxidase Enzyme.Violetta Mohos et al.International journal of molecular sciences, 20(11) (2019-06-05) 4-Methylcatechol, a Flavonoid Metabolite with Potent Antiplatelet Effects.Lenka Applová et al.Molecular nutrition & food research, 63(20), e1900261-e1900261 (2019-07-26) Inhibition of Cancer Cell Proliferation and Antiradical Effects of Decoction, Hydroalcoholic Extract, and Principal Constituents of Hemidesmus indicus R. Br.Giancarlo Statti et al.Phytotherapy research : PTR, 29(6), 857-863 (2015-03-11) Synthesis, biological evaluation and molecular docking studies of 1,3,4-oxadiazole derivatives as potential immunosuppressive agents.Zhi-Ming Zhang et al.Bioorganic & medicinal chemistry, 20(10), 3359-3367 (2012-04-24)

Remarks

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Name	CAS

Description

Properties

Safety

SDS

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