2-Methyl-2-propanesulfinamide - CAS 146374-27-8
Catalog: |
BB010080 |
Product Name: |
2-Methyl-2-propanesulfinamide |
CAS: |
146374-27-8 |
Synonyms: |
2-methylpropane-2-sulfinamide |
IUPAC Name: | 2-methylpropane-2-sulfinamide |
Description: | 2-Methyl-2-propanesulfinamide (CAS# 146374-27-8) is also used as a reagent in the synthetic preparation of amide series as BACE1 inhibitor and potential anti-Alzheimer's drug. |
Molecular Weight: | 121.20 |
Molecular Formula: | C4H11NOS |
Canonical SMILES: | CC(C)(C)S(=O)N |
InChI: | InChI=1S/C4H11NOS/c1-4(2,3)7(5)6/h5H2,1-3H3 |
InChI Key: | CESUXLKAADQNTB-UHFFFAOYSA-N |
Boiling Point: | 220 °C at 760 mmHg |
Purity: | 97.0 % |
Density: | 1.124 g/cm3 |
MDL: | MFCD05861480 |
LogP: | 1.97330 |
GHS Hazard Statement: | H301 (60%): Toxic if swallowed [Danger Acute toxicity, oral] |
Precautionary Statement: | P261, P264, P270, P271, P280, P301+P310, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
CN-113278023-B | Nitrogen-containing heterocyclic compound and preparation method and application thereof | 20210722 |
CN-113475740-A | Preparation method of chiral synthetic nicotine | 20210710 |
CN-113173860-A | Preparation method of 2-methylalanine | 20210517 |
CN-113337857-A | Acidic sulfate copper electroplating combined additive for thickening PCB through hole metal | 20210429 |
CN-113264839-A | Method for preparing levo-terbutaline by using chiral prosthetic group | 20210427 |
PMID | Publication Date | Title | Journal |
22553109 | 20120901 | Chiral sulfur compounds studied by Raman optical activity: tert-butanesulfinamide and its precursor tert-butyl tert-butanethiosulfinate | Chirality |
22694241 | 20120706 | Microwave-assisted solvent-free synthesis of enantiomerically pure N-(tert-butylsulfinyl)imines | The Journal of organic chemistry |
22566097 | 20120701 | The enantiomers of epiboxidine and of two related analogs: synthesis and estimation of their binding affinity at α4β2 and α7 neuronal nicotinic acetylcholine receptors | Chirality |
22458413 | 20120504 | Palladium-catalyzed C-N cross coupling of sulfinamides and aryl halides | The Journal of organic chemistry |
22480132 | 20120420 | Lewis acid promoted highly diastereoselective Petasis Borono-Mannich reaction: efficient synthesis of optically active β,γ-unsaturated α-amino acids | Organic letters |
Complexity: | 84.2 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 121.05613515 |
Formal Charge: | 0 |
Heavy Atom Count: | 7 |
Hydrogen Bond Acceptor Count: | 3 |
Hydrogen Bond Donor Count: | 1 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 121.05613515 |
Rotatable Bond Count: | 1 |
Topological Polar Surface Area: | 62.3 Å2 |
Undefined Atom Stereocenter Count: | 1 |
Undefined Bond Stereocenter Count: | 0 |
XLogP3: | 0 |
Online Inquiry
Customer Support
Customer Centered
Related Functional Groups
Sulfur Compounds
Customers Also Viewed
INDUSTRY LEADERS TRUST OUR PRODUCTS