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468037

Sigma-Aldrich

cis-1,4-二乙酰氧基-2-丁烯

95%

同義詞:

顺-1,4-二醋酸基-2-丁烯

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About This Item

線性公式:
CH3CO2CH2CH=CHCH2O2CCH3
CAS號碼:
25260-60-0
分子量：:
172.18
MDL號碼:
MFCD00059339
分類程式碼代碼:
12352100
PubChem物質ID:
24870459
NACRES:
NA.22

品質等級

100

化驗

95%

折射率

n20/D 1.443 (lit.)

bp

120-121 °C/18 mmHg (lit.)

密度

1.08 g/mL at 25 °C (lit.)

官能基

ester

SMILES 字串

[H]\C(COC(C)=O)=C(/[H])COC(C)=O

InChI

1S/C8H12O4/c1-7(9)11-5-3-4-6-12-8(2)10/h3-4H,5-6H2,1-2H3/b4-3-

InChI 密鑰

VZUAUHWZIKOMFC-ARJAWSKDSA-N

相關類別

一般說明

cis-1,4-Diacetoxy-2-butene is an ester. Ruthenium olefin metathesis catalysts having cyclic (alkyl)(amino)carbenes effectively catalyzes the cross-metathesis of cis-1,4-diacetoxy-2-butene with allylbenzene. cis-1,4-Diacetoxy-2-butene on pyrolysis affords 1-acetoxy-1,3-butadiene, a diacetate and an isomeric 1,2-diacetoxy-3-butene. Mechanism of pyrolysis has been investigated.

應用

cis-1,4-Diacetoxy-2-butene may be used in the preparation of hindered Diels-Alder adducts. It may be used for the synthesis of 1,2,3,4-tetrahydro-2-vinylquinoxalines, via Palladium-catalyzed tandem allylation of 1,2-phenylenediamines.

象形圖

Exclamation mark
GHS07

訊號詞

Warning

危險聲明

H315

危險分類

Skin Irrit. 2

儲存類別代碼

10 - Combustible liquids

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

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

從最近期的版本中選擇一個：

分析證明 (COA)

Lot/Batch Number
MKCQ0672
MKCG8741
MKCG4280
MKCD0680
MKCD0681

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Kerstin Rosmarion et al.
Applied spectroscopy, 59(3), 366-375 (2005-05-20)
Hindered Diels-Alder adducts have been prepared from 3,6-dibromophencyclone, 2, with cis-1,4-diacetoxy-2-butene, 3; cis-2-butene-1,4-diol, 4; and N-benzylmaleimide, 5. The adduct from the parent phencyclone, 1, with N-benzylmaleimide was prepared for comparison. One- and two-dimensional (1D and 2D) proton and carbon-13 NMR
Pyrolysis of Esters. V. Mechanism of 1, 4-Elimination1.
Bailey WJ and BARCLAY Jr R.
The Journal of Organic Chemistry, 21(3), 328-331 (1956)
Donde R Anderson et al.
Organometallics, 27(4), 563-566 (2008-06-28)
The evaluation of ruthenium olefin metathesis catalysts 4-6 bearing cyclic (alkyl)(amino)carbenes (CAACs) in the cross-metathesis of cis-1,4-diacetoxy-2-butene (7) with allylbenzene (8) and the ethenolysis of methyl oleate (11) is reported. Relative to most NHC-substituted complexes, CAAC-substituted catalysts exhibit lower E/Z
Palladium-catalyzed tandem allylation of 1, 2-phenylenediamines with cis-1, 4-diacetoxy-2-butene.
Yang SC, et al.
Tetrahedron Letters, 45(25), 4951-4954 (2004)

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