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Chemical structure of CAS 19158-51-1

p-Toluenesulphonyl cyanide

In Stock•Starting at $8 for 100 mg•Purity ≥ 98%
CAS No.19158-51-1
MDL No.MFCD00009977
MFC8H7NO2S
MW181.21
InChI KeyJONIMGVUGJVFQD-UHFFFAOYSA-N
CUSTOM SYNTHESIS

Pricing & Availability

Pack SizePurityPriceAvailabilityAction
100 mg98%$8In Stock
250 mg98%$9In Stock
1 g98%$13In Stock
5 g98%$35In Stock
10 g98%$67In Stock
25 g98%$139In Stock
4*25 g98%$542In Stock
Custom synthesis and bulk supply options are available upon request.

Product Information

CAS No.19158-51-1
Product Namep-Toluenesulphonyl cyanide
CorrosiveCorrosive
IrritantIrritant
Signal Word:Danger
HCode:H312-H314-H318-H332
PCode:P260-P261-P264-P264+P265-P271-P280-P301+P330+P331-P302+P352-P302+P361+P354-P304+P340-P305+P354+P338-P316-P317-P321-P362+P364-P363-P405-P501

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Studies related to this compound and its mechanism of action

Photochemically induced radical transformation of C(sp3)-H bonds to C(sp3)-CN bonds.

Organic letters • Vol. 13, Issue 21 • 2011
PMID: 21992181DOI: 10.1021/ol202659e

Click azide-nitrile cycloaddition as a new ligation tool for the synthesis of tetrazole-tethered C-glycosyl alpha-amino acids.

The Journal of organic chemistry • Vol. 73, Issue 24 • 2008
PMID: 18847242DOI: 10.1021/jo801670k

Mild cobalt-catalyzed hydrocyanation of olefins with tosyl cyanide.

Angewandte Chemie (International ed. in English) • Vol. 46, Issue 24 • 2007
PMID: 17479996DOI: 10.1002/anie.200700575

Synthesis of 3-substituted bicyclic imidazo[1,2-d][1,2,4]thiadiazoles and tricyclic benzo[4,5]imidazo[1,2-d][1,2,4]thiadiazoles.

The Journal of organic chemistry • Vol. 70, Issue 16 • 2005
PMID: 16050682DOI: 10.1021/jo0507486

Documentation

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