146374-27-8
146374-27-8
Chemical Structure
2-Methylpropane-2-sulfinamide
- CAS No.: 146374-27-8
- Formula:C4H11NOS
- Molecular Weight:121.20
IUPAC Name: 2-methylpropane-2-sulfinamide
InChIKey: CESUXLKAADQNTB-UHFFFAOYSA-N
SMILES: CC(S(N)=O)(C)C
Biological Activity: 2-Methylpropane-2-sulfinamide is an amide compound that can be used as an intermediate in pharmaceutical synthesis.
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
2-Methylpropane-2-sulfinamide | 98.0% | 2-Methylpropane-2-sulfinamide is an amide compound that can be used as an intermediate in pharmaceutical synthesis. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Potassium tert-butoxide | 99.98% | Potassium tert-butoxide (Potassiumtbutoxide) is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
(R)-(+)-tert-Butylsulfinamide | 99.95% | (R)-(+)-tert-Butylsulfinamide ((R)-2-Methylpropane-2-sulfinamide) is a chiral reagent commonly used in the asymmetric synthesis of compounds such as amines, amino acids, and amino alcohols. (R)-(+)-tert-Butylsulfinamide achieves stereoselective reactions by condensing with carbonyl groups to form sulfinyl imine intermediates, and after the reaction, this group can be removed under acidic conditions to obtain the target product. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
(S)-(-)-tert-Butylsulfinamide | 99.94% | (S)-(-)-tert-Butylsulfinamide (S-(-)-T-Butylsulfinimide) is a compound containing a chiral sulfur atom. (S)-(-)-tert-Butylsulfinamide can be used in the synthesis of other compounds. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
3,3-Dimethyl-1-butanol | 99.19% | 3,3-Dimethyl-1-butanol (DMB) is an orally active inhibitor of trimethylamine (TMA) and trimethylamine N-oxide (TMAO). 3,3-Dimethyl-1-butanol inhibits the signaling pathway of p65 NF-κB and TGF-β1/Smad3. 3,3-Dimethyl-1-butanol has potential applications in cardiovascular disease (CVD). | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
2-Amino-2-methylpropan-1-ol hydrochloride | 97.0% | 2-Amino-2-methylpropan-1-ol hydrochloride is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Dimethyl sulfoxide-13C2 | Dimethyl sulfoxide-13C2 (DMSO-13C2) is the 13C-labeled Dimethyl sulfoxide (HY-Y0320C). Dimethyl sulfoxide (DMSO) is an aprotic solvent that can dissolve water-insoluble therapeutic and toxic agents. Dimethyl sulfoxide (DMSO) has a strong affinity for water and has the ability to rapidly penetrate or enhance the penetration of?other?substances through biological membranes. Dimethyl sulfoxide also has potential free radical scavenging and anticholinesterase effects and may affect coagulation activity. Dimethyl sulfoxide also induces histamine release from mast cells but is thought to have low systemic toxicity. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Dimethyl sulfoxide | 99.98% | Dimethyl sulfoxide (DMSO) is an aprotic solvent that can dissolve water-insoluble therapeutic and toxic agents. Dimethyl sulfoxide (DMSO) has a strong affinity for water and has the ability to rapidly penetrate or enhance the penetration of other substances through biological membranes. Dimethyl sulfoxide also has potential free radical scavenging and anticholinesterase effects and may affect coagulation activity. Dimethyl sulfoxide also induces histamine release from mast cells but is thought to have low systemic toxicity. Low endotoxin, can be used in various biochemical experiments such as drug dissolution. |
||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
Trimethylacetaldehyde | Trimethylacetaldehyde (Pivalic aldehyde; Pivalaldehyde) is an inhibitor of E. coli betaine aldehyde dehydrogenase (ALDH) with a Ki of 4.5 mM. Trimethylacetaldehyde serves as a substrate for Drosophila melanogaster alcohol dehydrogenase (AdhS), undergoing oxidation and disproportionation reactions with the release of NADH, and also forms an inactive binary enzyme-aldehyde complex via a compulsory ordered reaction mechanism. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
