Dimethyl 3,3'-Thiodipropionate, 98%

Name: Dimethyl 3,3'-Thiodipropionate, 98% | 4131-74-2
Brand: J&K Chemical
SKU: JK324493_500_ML
Price: 86.5 USD
Availability: OutOfStock

Cat. No JK324493_500_ML

Vendor: J&K Chemical

Product Information

Product Name

Dimethyl 3,3'-Thiodipropionate, 98%

Brand Name

J&K

Product Number

324493

CAS

4131-74-2

Molecular Formula

C8H14O4S

Molecular Weight

206.26

SDS Document

View/Download

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

3,3'-Thiodipropionic Acid Dimethyl Ester

PubChem CID

77781

IUPAC Name

methyl 3-(3-methoxy-3-oxopropyl)sulfanylpropanoate

InChI Key

MYWWWNVEZBAKHR-UHFFFAOYSA-N

SMILES

COC(=O)CCSCCC(=O)OC

Properties

Density

1.1615

Boiling Point

164

n20D

1.4740-1.4760

References Data Source From Pubchem

Recent Updates on Morpholino Pyrimidine Derivatives as Promising PI3K/Akt/mTOR Inhibitors

Publication Name: Chemistry Africa

Publication Date: 2024-12-26

DOI: 10.1007/s42250-024-01163-2

Synthesis and characterization of sulfide, sulfoxide and sulfone derivatives of thiopyran: antimicrobial evaluation

Publication Name: Research on Chemical Intermediates

Publication Date: 2017-07-24

DOI: 10.1007/s11164-017-3075-4

By Dieckmann Condensation

Publication Name: Science of Synthesis

Publication Date: 2008

Simple and Efficient Preparation of Reagents for Thiopyran Introduction: Methyl Tetrahydro-4-oxo-2H-thiopyran-3-carboxylate, Tetrahydro-4H-thiopyran-4-one, and 3,6-Dihydro-4-trimethylsilyloxy-2H-thiopyran

Publication Name: Synthesis

Publication Date: 2007-02-28

DOI: 10.1055/s-2007-965954

Dimethyl 3,3'-Thiodipropionate, 98%

Product Information

General Information

Properties

References Data Source From Pubchem

Recent Updates on Morpholino Pyrimidine Derivatives as Promising PI3K/Akt/mTOR Inhibitors

Synthesis and characterization of sulfide, sulfoxide and sulfone derivatives of thiopyran: antimicrobial evaluation

By Dieckmann Condensation

Simple and Efficient Preparation of Reagents for Thiopyran Introduction: Methyl Tetrahydro-4-oxo-2H-thiopyran-3-carboxylate, Tetrahydro-4H-thiopyran-4-one, and 3,6-Dihydro-4-trimethylsilyloxy-2H-thiopyran

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