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Merck

79408

Sigma-Aldrich

磷腈配体 P1-叔丁基

≥97.0% (GC)

别名:

N′-叔丁基-N,N,N′,N′,N″,N″-六甲基亚氨代磷酸三酰胺, 叔丁基亚氨基-三(二甲氨基)正膦

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About This Item

经验公式(希尔记法):
C10H27N4P
CAS号:
分子量:
234.32
Beilstein:
4178783
MDL號碼:
分類程式碼代碼:
12352001
PubChem物質ID:
NACRES:
NA.22

化驗

≥97.0% (GC)

形狀

liquid

SMILES 字串

CN(C)P(N(C)C)(N(C)C)=NC(C)(C)C

InChI

1S/C10H27N4P/c1-10(2,3)11-15(12(4)5,13(6)7)14(8)9/h1-9H3

InChI 密鑰

YRNOSHBJMBLOSL-UHFFFAOYSA-N

其他說明

与BEMP具有相似碱性的空间位阻中性氮碱(货号20025);用POCl3或P4O10将氨基甲酸根阴离子脱水成异氰酸酯的碱

象形圖

Health hazardCorrosion

訊號詞

Danger

危險聲明

危險分類

Carc. 1B - Eye Dam. 1 - Muta. 1B - Skin Corr. 1B

儲存類別代碼

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

水污染物質分類(WGK)

WGK 3

閃點(°F)

235.4 °F - closed cup

閃點(°C)

113 °C - closed cup

個人防護裝備

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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T.E. Waldman et al.
Journal of the Chemical Society. Chemical Communications, 957-957 (1994)
Lan-Fang Hu et al.
Molecules (Basel, Switzerland), 25(2) (2020-01-16)
The copolymerization of biorenewable succinic anhydride (SA) with propylene oxide (PO) is a promising way to synthesize biodegradable aliphatic polyesters. However, the catalytic systems for this reaction still deserve to be explored because the catalytic activity of the reported catalysts
R. Schwesinger et al
Angewandte Chemie (International Edition in English), 105, 1420-1420 (1994)

商品

Phosphazene base reagents are available as monomeric (P1 and BEMP), dimeric (P2), and tetrameric (P4) bases with different side chains to control their sterical hindrance.

Phosphazene base reagents are available as monomeric (P1 and BEMP), dimeric (P2), and tetrameric (P4) bases with different side chains to control their sterical hindrance.

Phosphazene base reagents are available as monomeric (P1 and BEMP), dimeric (P2), and tetrameric (P4) bases with different side chains to control their sterical hindrance.

Phosphazene base reagents are available as monomeric (P1 and BEMP), dimeric (P2), and tetrameric (P4) bases with different side chains to control their sterical hindrance.

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