HomeProductsBuilding BlocksFunctional GroupsSulfonyl ChloridesCAS 31562-43-3
Chemical structure of CAS 31562-43-3

2-Methylpropane-2-sulfinyl chloride

In Stock•Starting at $18 for 100 mg•Purity ≥ 97%
CAS No.31562-43-3
MDL No.MFCD04974074
MFC4H9ClOS
MW140.63
InChI KeyZLJKQOWJEZSNBE-UHFFFAOYSA-N
CUSTOM SYNTHESIS

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
100 mg>97%$18In Stock
250 mg>97%$19In Stock
1 g>97%$23In Stock
5 g98%$65In Stock
10 g98%$125In Stock
25 g98%$274In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

CAS No.31562-43-3
Product Name2-Methylpropane-2-sulfinyl chloride
FlammableFlammable
CorrosiveCorrosive
Signal Word:Danger
HCode:H226-H314
PCode:P210-P233-P240-P241-P242-P243-P260-P264-P280-P301+P330+P331-P302+P361+P354-P303+P361+P353-P304+P340-P305+P354+P338-P316-P321-P363-P370+P378-P403+P235-P405-P501

Related Articles

Studies related to this compound and its mechanism of action

Recycling the tert-butanesulfinyl group in the synthesis of amines using tert-butanesulfinamide.

The Journal of organic chemistry • Vol. 74, Issue 7 • 2009
PMID: 19323570DOI: 10.1021/jo9001883

Catalytic enantioselective sulfinyl transfer using cinchona alkaloid catalysts.

Organic letters • Vol. 7, Issue 9 • 2005
PMID: 15844893DOI: 10.1021/ol050275p

Palladium-catalyzed enantioselective 1,3-rearrangement of racemic allylic sulfinates: asymmetric synthesis of allylic sulfones and kinetic resolution of an allylic sulfinate.

The Journal of organic chemistry • Vol. 69, Issue 8 • 2004
PMID: 15074920DOI: 10.1021/jo030340d

Catalytic enantioselective synthesis of sulfinate esters through the dynamic resolution of tert-butanesulfinyl chloride.

Journal of the American Chemical Society • Vol. 126, Issue 26 • 2004
PMID: 15225052DOI: 10.1021/ja047845l

Documentation

Similar Products