Dimedone, 98%

Name: Dimedone, 98% | 126-81-8
Brand: J&K Chemical
SKU: JK439198_100_G
Price: 60.8 USD
Availability: OutOfStock

Cat. No JK439198_100_G

Vendor: J&K Chemical

Product Information

Product Name

Dimedone, 98%

Brand Name

J&K

Product Number

439198

CAS

126-81-8

Molecular Formula

C8H12O2

Molecular Weight

140.18

Certificate of Analysis (COA)

COA not found

General Information

Synonyms

Methone

PubChem CID

31358

IUPAC Name

5,5-dimethylcyclohexane-1,3-dione

InChI Key

BADXJIPKFRBFOT-UHFFFAOYSA-N

SMILES

CC1(CC(=O)CC(=O)C1)C

Properties

Melting Point

146-148

Boiling Point

164-166

References Data Source From Pubchem

Defining and refining the cysteine redoxome through sulfur chemical biology

Publication Name: Nature Chemical Biology

Publication Date: 2026-02-27

DOI: 10.1038/s41589-026-02145-w

Material to synthetic efficiency: Novel AMP modified g-C3N4·SO3H catalyst for the green and scalable synthesis of xanthene-1,8-diones

Publication Name: Research on Chemical Intermediates

Publication Date: 2026-02-26

DOI: 10.1007/s11164-026-05952-x

Phthalazine scaffolds in medicinal chemistry: a review of their synthesis, versatility, and pharmacological significance

Publication Name: Molecular Diversity

Publication Date: 2026-02-25

DOI: 10.1007/s11030-026-11489-3

One-pot synthesis of 1,8-dioxo-decahydroacridines and 1,8-dioxo- octahydroxanthene derivatives using novel biopolymer xanthan perchloric acid (XPA) catalyst

Publication Name: Research on Chemical Intermediates

Publication Date: 2026-02-15

DOI: 10.1007/s11164-026-05941-0

Beta-irradiation of biomass in the presence of 1-alkyl-3-methyl-imidazolium ionic liquids: model compound reactions to clarify the reaction at the reducing end of aldoses and cellulose

Publication Name: Cellulose

Publication Date: 2026-02-10

DOI: 10.1007/s10570-026-06962-z

Dimedone, 98%

Product Information

General Information

Properties

References Data Source From Pubchem

Defining and refining the cysteine redoxome through sulfur chemical biology

Material to synthetic efficiency: Novel AMP modified g-C3N4·SO3H catalyst for the green and scalable synthesis of xanthene-1,8-diones

Phthalazine scaffolds in medicinal chemistry: a review of their synthesis, versatility, and pharmacological significance

One-pot synthesis of 1,8-dioxo-decahydroacridines and 1,8-dioxo- octahydroxanthene derivatives using novel biopolymer xanthan perchloric acid (XPA) catalyst

Beta-irradiation of biomass in the presence of 1-alkyl-3-methyl-imidazolium ionic liquids: model compound reactions to clarify the reaction at the reducing end of aldoses and cellulose

Dimedone, 98%

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-3-methoxy-L-phenylalanine

2-Ethynyl-1,3,5-trimethylbenzene, 97%

Tris-acetic acid electrophoresis buffer (50×TAE)

[S(R)]-N-[(1S)-1-[2-(Diadamantanphosphino)phenyl]ethyl]-N,2-dimethyl-2-propanesulfinamide, 95%

Mycophenolate Mofetil EP Impurity H

3-(4-Bromo-2-fluoro-3-methoxyphenyl)-3-oxo-propionic acid ethyl ester

Isochroman-1-carboxylic acid

Mycophenolate Mofetil

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Dimedone, 98%

Product Information

General Information

Properties

References Data Source From Pubchem

Defining and refining the cysteine redoxome through sulfur chemical biology

Material to synthetic efficiency: Novel AMP modified g-C3N4·SO3H catalyst for the green and scalable synthesis of xanthene-1,8-diones

Phthalazine scaffolds in medicinal chemistry: a review of their synthesis, versatility, and pharmacological significance

One-pot synthesis of 1,8-dioxo-decahydroacridines and 1,8-dioxo- octahydroxanthene derivatives using novel biopolymer xanthan perchloric acid (XPA) catalyst

Beta-irradiation of biomass in the presence of 1-alkyl-3-methyl-imidazolium ionic liquids: model compound reactions to clarify the reaction at the reducing end of aldoses and cellulose

Dimedone, 98%

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2-Ethynyl-1,3,5-trimethylbenzene, 97%

Tris-acetic acid electrophoresis buffer (50×TAE)

[S(R)]-N-[(1S)-1-[2-(Diadamantanphosphino)phenyl]ethyl]-N,2-dimethyl-2-propanesulfinamide, 95%

Mycophenolate Mofetil EP Impurity H

3-(4-Bromo-2-fluoro-3-methoxyphenyl)-3-oxo-propionic acid ethyl ester

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Mycophenolate Mofetil

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