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| 3,3-Dimethylglutaric acid Basic information |
| Product Name: | 3,3-Dimethylglutaric acid | | Synonyms: | 3,3-dimethyl-pentanedioicaci;Glutaric acid, 3,3-dimethyl-;Pentanedioic acid, 3,3-dimethyl-;3,3-DIMETHYLPENTANEDIOIC ACID;3,3-DIMETHYLPENTANEDOIC ACID;3,3-DIMETHYLGLUTARIC ACID;2,2-O-DIMETHYLPROPANE-1,3-DICARBOXYLIC ACID;2,2-DIMETHYLPROPANE-1,3-DICARBOXYLIC ACID | | CAS: | 4839-46-7 | | MF: | C7H12O4 | | MW: | 160.17 | | EINECS: | 225-425-0 | | Product Categories: | Organic acids | | Mol File: | 4839-46-7.mol |
| 3,3-Dimethylglutaric acid Chemical Properties |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-36 | | WGK Germany | 3 | | TSCA | Yes | | HS Code | 29171990 |
| 3,3-Dimethylglutaric acid Usage And Synthesis |
| Chemical Properties | white to beige fine crystalline powder | | Uses | 3,3-Dimethylglutaric acid can be used as reactant involved in: Cyclodehydration of diols; Synthesis of conjugates of betulin derivatives used as anti-HIV agents; Preparation of dimeric peptide antagonists of IgG-FcRn interaction; Microwave-assisted protection of glutaraldehyde; Synthesis of glycyrrhetinic acid derivatives for proteasome inhibition; Catalytic, asymmetric transannular aldolizations.
| | Uses | 3,3-Dimethylglutaric Acid is a versatile reactant used in the synthesis of (+)-Hirsutene via catalytic asymmetric transannular aldolization. | | Uses | Reactant involved in:- Cyclodehydration of diols
- Synthesis of conjugates of betulin derivatives used as anti-HIV agents
- Preparation of dimeric peptide antagonists of IgG-FcRn interaction
- Microwave-assisted protection of glutaraldehyde
- Synthesis of glycyrrhetinic acid derivatives for proteasome inhibition
- Catalytic, asymmetric transannular aldolizations
| | Definition | ChEBI: An alpha,omega-dicarboxylic acid that is glutaric acid substituted by two methyl groups at the C-3 position. |
| 3,3-Dimethylglutaric acid Preparation Products And Raw materials |
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