196929-78-9

  • Product Name:(R)-(+)-2-Methyl-2-propanesulfinamide
  • Molecular Formula:C4H11NOS
  • Molecular Weight:121.203
  • Appearance:white to light yellow crystal powder
Inquiry

Product Details

pd_meltingpoint:103-107 °C(lit.)

Appearance:white to light yellow crystal powder

Purity:99%

Manufacturer supply top purity (R)-(+)-2-Methyl-2-propanesulfinamide 196929-78-9 with ISO standards

  • Molecular Formula:C4H11NOS
  • Molecular Weight:121.203
  • Appearance/Colour:white to light yellow crystal powder 
  • Melting Point:103-107 °C(lit.) 
  • Refractive Index:4 ° (C=1, CHCl3) 
  • Boiling Point:219.957 °C at 760 mmHg 
  • PKA:10.11±0.50(Predicted) 
  • Flash Point:86.827 °C 
  • PSA:62.30000 
  • Density:1.124 g/cm3 
  • LogP:1.97330 

(R)-(+)-2-Methyl-2-propanesulfinamide(Cas 196929-78-9) Usage

InChI:InChI=1/C6H17NS.H2O/c1-6(2,3)8(4,5)7;/h7H2,1-5H3;1H2

196929-78-9 Relevant articles

Improved synthesis of tert-butanesulfinamide suitable for large-scale production

Weix, Daniel J.,Ellman, Jonathan A.

, p. 1317 - 1320 (2003)

(Matrix presented) An improved synthesis...

Catalytic asymmetric oxidation of tert-butyl disulfide. Synthesis of tert-butanesulfinamides, tert-butyl sulfoxides, and tert-butanesulfinimines

Cogan, Derek A.,Liu, Guangcheng,Kim, Kyungjin,Backes, Bradley J.,Ellman, Jonathan A.

, p. 8011 - 8019 (1998)

The first example of the catalytic asymm...

Method for preparing chiral tert-butyl sulfinamide

-

Paragraph 0021; 0026-0027, (2021/01/30)

The invention belongs to the technical f...

Method of synthesizing enantiomerically pure tert-butanesulfinamide

-

Paragraph 0058-0059, (2018/09/11)

The invention discloses a method of synt...

Method for preparing enantiomer pure methylpropane-2-sulfinamide

-

Paragraph 0015; 0058; 0059, (2018/09/29)

The invention discloses a method for pre...

Method for preparing pure enantio-methylpropane-2-sulfinamide

-

Paragraph 0015; 0041; 0058; 0059, (2018/10/19)

The invention discloses a method for pre...

196929-78-9 Process route

2-Methyl-propane-2-sulfinic acid ((R)-3-[1,3]dioxan-2-yl-1-phenyl-propyl)-amide
860640-13-7

2-Methyl-propane-2-sulfinic acid ((R)-3-[1,3]dioxan-2-yl-1-phenyl-propyl)-amide

2-phenyl-3,4-dihydro-2<i>H</i>-pyrrole

2-phenyl-3,4-dihydro-2H-pyrrole

(R)-2-methylpropane-2-sulfinamide
196929-78-9

(R)-2-methylpropane-2-sulfinamide

trimethyleneglycol
504-63-2

trimethyleneglycol

Conditions
Conditions Yield
With trifluoroacetic acid-d1; In water-d2; for 0.25h;
2,2,2-trifluoro-1-phenylethyl 2-methylpropane-2-sulfinate

2,2,2-trifluoro-1-phenylethyl 2-methylpropane-2-sulfinate

1-phenyl-2,2,2-trifluoromethylethanol
340-04-5,340-05-6

1-phenyl-2,2,2-trifluoromethylethanol

(R)-2-methylpropane-2-sulfinamide
196929-78-9

(R)-2-methylpropane-2-sulfinamide

Conditions
Conditions Yield
With lithium hexamethyldisilazane; In tetrahydrofuran; at 0 - 20 ℃; for 10h; Inert atmosphere;

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