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Merck

311022

Sigma-Aldrich

二(2-吡啶)硫代碳酸酯

98%

别名:

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

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About This Item

经验公式(希尔记法):
C11H8N2O2S
CAS号:
分子量:
232.26
Beilstein:
4314435
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

98%

mp

94-98 °C (lit.)

儲存溫度

−20°C

SMILES 字串

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 密鑰

IKYOVSVBLHGFMA-UHFFFAOYSA-N

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應用

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.

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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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

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