Skip to Content
MilliporeSigma
All Photos(1)

Documents

311022

Sigma-Aldrich

Di(2-pyridyl) thionocarbonate

98%

Synonym(s):

Di-2-pyridyl thionocarbonate, O,O-Di(2-pyridinyl) thiocarbonate, O,O-Di(pyridin-2-yl) carbonothioate, O,O′-Di(pyridin-2-yl) carbonothioate, Thiocarbonic acid di-O,O-(2-pyridyl) ester

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C11H8N2O2S
CAS Number:
Molecular Weight:
232.26
Beilstein/REAXYS Number:
4314435
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

98%

mp

94-98 °C (lit.)

storage temp.

−20°C

SMILES string

S=C(Oc1ccccn1)Oc2ccccn2

InChI

1S/C11H8N2O2S/c16-11(14-9-5-1-3-7-12-9)15-10-6-2-4-8-13-10/h1-8H

InChI key

IKYOVSVBLHGFMA-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

Di-2-pyridyl thionocarbonate (DPT) was used in the synthesis of 10-des(carbamoyloxy)-10-isothiocyanatoporfiromycin. It was also used as a substitute of thiophosgene, a highly toxic agent, in the preparation of isothiocyanate.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

N Huh et al.
Bioconjugate chemistry, 7(6), 659-669 (1996-11-01)
Mitomycin C (1) is the prototypical bioreductive alkylating agent. Studies have shown that mitomycin C and its derivatives selectively alkylate guanine residues within di- and trinucleotide DNA sequences. This investigation sought to improve the selective DNA bonding properties of the
Mariarita Barone et al.
Molecular diversity, 17(3), 445-458 (2013-04-27)
The aim of this work was to evaluate the potential anti-inflammatory activity of eleven (5-15) new synthesized derivatives of benzo-thieno[3,2-d]pyrimidine on two cell models, namely human keratinocytes NCTC 2544 and mouse monocyte-macrophages J774. For the synthesis of test compounds an

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service