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Merck
CN

384267

3-丁烯酸甲酯

95%

别名:

乙烯基乙酸甲酯

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线性分子式:
CH2=CHCH2COOCH3
化学文摘社编号:
分子量:
100.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
223-076-9
Beilstein/REAXYS Number:
1741732
MDL number:
Assay:
95%
Form:
liquid
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产品名称

3-丁烯酸甲酯, 95%

InChI key

GITITJADGZYSRL-UHFFFAOYSA-N

InChI

1S/C5H8O2/c1-3-4-5(6)7-2/h3H,1,4H2,2H3

SMILES string

COC(=O)CC=C

assay

95%

form

liquid

refractive index

n20/D 1.409 (lit.)

bp

112 °C (lit.)

density

0.939 g/mL at 25 °C (lit.)

functional group

allyl
ester

Quality Level

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Application

3-丁烯酸甲酯可用于使用分子间烯烃交叉复分解法合成二肽烯烃等排体。

General description

3-丁烯酸甲酯是一种烯烃酯。据报道,它经过铁羰基促进异构化得到 α, β-不饱和酯。是 (-) 可卡因闪速真空热分解过程中形成的反应产物之一。报道了 3-丁烯酸甲酯的 H 2 和 CH 4 化学电离质谱。

pictograms

Flame

signalword

Danger

hcodes

pcodes

Hazard Classifications

Flam. Liq. 2

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

68.0 °F - closed cup

flash_point_c

20 °C - closed cup

ppe

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

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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The flash vacuum thermolysis of (-)-cocaine.
Sisti NJ, et al.
Tetrahedron Letters, 30(44), 5977-5980 (1989)
Site of protonation in the chemical ionization mass spectra of olefinic methyl esters.
Harrison AX and Ichikawa H.
Org. Mass Spectrom., 15(5), 244-248 (1980)
Rachel Chapla et al.
Polymers, 12(12) (2020-12-20)
Local mechanical stiffness influences cell behavior, and thus cell culture scaffolds should approximate the stiffness of the tissue type from which the cells are derived. In synthetic hydrogels, this has been difficult to achieve for very soft tissues such as
Kuo-Chen Shih et al.
The Journal of organic chemistry, 61(22), 7784-7792 (1996-11-01)
Ultraviolet photolysis of stoichiometric amounts of methyl oleate and Fe(CO)(5) in hexanes solvent at 0 degrees C gives Fe(CO)(3)(eta(4)-alpha,beta-ester) in which the alpha,beta-unsaturated ester isomer of methyl oleate is stabilized by eta(4)-oxadiene pi coordination of the olefin and ester carbonyl
Melissa M Vasbinder et al.
The Journal of organic chemistry, 67(17), 6240-6242 (2002-08-17)
An approach to the synthesis of dipeptide olefin isosteres using intermolecular olefin cross-metathesis is presented. In particular, a synthesis of the Pro-Gly isostere (1) is reported. Conversion of N-BOC-proline into the corresponding vinyl-substituted carbamate provides the N-terminal cross-metathesis partner (2).

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