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Merck

531820

Sigma-Aldrich

N,N′-二-Boc-硫脲

97%

别名:

N,N′-二-(叔丁氧基羰基)硫脲, N,N′-双-叔丁氧羰基硫脲

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About This Item

线性分子式:
((CH3)3COCONH)2CS
分子量:
276.35
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

97%

mp

131-135 °C (lit.)

官能基

amine
thiourea

SMILES 字串

CC(C)(C)OC(=O)NC(=S)NC(=O)OC(C)(C)C

InChI

1S/C11H20N2O4S/c1-10(2,3)16-8(14)12-7(18)13-9(15)17-11(4,5)6/h1-6H3,(H2,12,13,14,15,18)

InChI 密鑰

CSOJECDGWHHWRS-UHFFFAOYSA-N

一般說明

N,N′-Di-Boc-thiourea (N,N′-di-Boc-substituted thiourea), also known as di-Boc-thiourea is a thioacylating agent for preparing thiocarbonyl compounds.

應用

N,N′-Di-Boc-thiourea (di-Boc protected thiourea) may be used as a guanylating agent for the synthesis of guanidines, via guanylation of amines in the presence of Mukaiyama′s reagent as a promoter.

儲存類別代碼

13 - Non 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

Eyeshields, Gloves, type N95 (US)


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分析证书(COA)

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Recent developments in guanylating agents.
Katritzky AR and Rogovoy BV.
ARKIVOC (Gainesville, FL, United States), 4, 49-87 (2005)
N, N'-Di-Boc-substituted thiourea as a novel and mild thioacylating agent applicable for the synthesis of thiocarbonyl compounds.
Yin BL, et al.
Synthesis, 2010(06), 991-999 (2010)

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