4-Benzyl-2-methyl-1,2,4-thiadiazolidine-3,5-dione

Basic Information

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CAS Number

327036-89-5

Molecular Formula

C10H10N2O2S

Molecular Weight

222.27 g/mol

Chemical Classification

Basic Chemical Raw Materials Organic Chemicals Carboxylic Acids

Basic Chemical Raw Materials Organic Chemicals Heterocyclic Compounds

Pharmaceutical Chemicals Pharmaceutical Intermediates Heterocyclic Intermediates

Fine Chemicals Dyes and Pigments Organic Dyes

Basic Physical Properties

Melting Point

61.0 to 65.0 deg-C

Boiling Point

335.5°C at 760 mmHg

Solubility

DMSO: 18 mg/mL

SMILES

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CN1C(=O)N(C(=O)S1)CC2=CC=CC=C2

InChI

InChI=1S/C10H10N2O2S/c1-11-9(13)12(10(14)15-11)7-8-5-3-2-4-6-8/h2-6H,7H2,1H3

InChIKey

JDSJDASOXWCHPN-UHFFFAOYSA-N

LogP

0.6567999999999993

Topological Polar Surface Area

44.0 Å²

Hydrogen Bond Donor/Acceptor

0 / 4

Complexity

277

Safety Information

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GHS Hazard Pictograms

H334

Hazard Statement

H334 May cause allergy or asthma symptoms or breathing difficulties if inhaled
Sensitization, respiratory

Synonyms & References

English

TDZD8
AKOS016004653
SCHEMBL139834
NCGC00165913-01
NCGC00165913-03
A875545
AC-35779
TDZD-8
Thiadiazolidinone (TDZD) deriv. 8
CHEBI:147411
GTPL5977
CS-1671
BDBM7781
HY-11012
4-Benzyl-2-methyl-[1,2,4]thiadiazolidine-3,5-dione
GSK-3 beta Inhibitor I
CCG-206841
GSK-3beta Inhibitor I - CAS 327036-89-5
J-514480
EX-A109
U3W
JDSJDASOXWCHPN-UHFFFAOYSA-N
GSK-3beta Inhibitor I
2-methyl-4-(phenylmethyl)-1,2,4-thiadiazolidine-3,5-dione
NP 01139
Q27077898
thiadiazolidinone-8
4-Benzyl-2-methyl-1,2,4-thiadiazolidine-3,5-dione
BCP07657
GSK-3
A Inhibitor I;NP 01139

MDL Number

MFCD04973552

Customs Code

2934999090

FAQ

What regulatory guidelines apply to 4-Benzyl-2-methyl-1,2,4-thiadiazolidine-3,5-dione (CAS: 327036-89-5)?

4-Benzyl-2-methyl-1,2,4-thiadiazolidine-3,5-dione (CAS: 327036-89-5) is regulated under various guidelines including REACH for EU manufacturers and importers, GHS for global chemical safety classification, and FDA/EPA for pharmaceutical and environmental safety. Proper labeling, storage, and handling practices are required to comply with these regulations.

Are there alternatives to 4-Benzyl-2-methyl-1,2,4-thiadiazolidine-3,5-dione in synthesis?

Several alternatives can be used in the synthesis of 4-Benzyl-2-methyl-1,2,4-thiadiazolidine-3,5-dione, such as 1,3-benzothiazolidine-2,4-dione and 1,2,4-thiadiazolidine-3,5-dione. These alternatives may offer different reactivity and selectivity profiles, and should be chosen based on the specific application and desired properties.

What is the market or research trend for 4-Benzyl-2-methyl-1,2,4-thiadiazolidine-3,5-dione?

The research trend for 4-Benzyl-2-methyl-1,2,4-thiadiazolidine-3,5-dione indicates increasing interest in its use as a stabilizer in pharmaceuticals and as a precursor in the synthesis of other thiadiazolidine derivatives. Market demand is likely to grow with advancements in drug development and materials science, driven by its unique chemical properties.

How should waste containing 4-Benzyl-2-methyl-1,2,4-thiadiazolidine-3,5-dione be handled?

Waste containing 4-Benzyl-2-methyl-1,2,4-thiadiazolidine-3,5-dione should be collected in appropriate containers and disposed of through professional waste disposal services. Incineration is a common method, but environmental precautions must be taken to prevent air pollution. Ensure compliance with local and international waste management regulations to protect the environment and human health.