194328
Ethyl 3,3-dimethylacrylate
98%
Sinônimo(s):
Ethyl 3-methylcrotonate
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About This Item
Fórmula linear:
(CH3)2C=CHCO2C2H5
Número CAS:
Peso molecular:
128.17
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Ensaio
98%
Formulário
liquid
índice de refração
n20/D 1.436 (lit.)
p.e.
154-155 °C (lit.)
densidade
0.922 g/mL at 25 °C (lit.)
grupo funcional
ester
cadeia de caracteres SMILES
CCOC(=O)\C=C(\C)C
InChI
1S/C7H12O2/c1-4-9-7(8)5-6(2)3/h5H,4H2,1-3H3
chave InChI
UTXVCHVLDOLVPC-UHFFFAOYSA-N
Categorias relacionadas
Descrição geral
Ion-molecule reactions between the O=P(OCH3)2+phosphonium ions and ethyl 3,3-dimethylacrylate has been investigated by quadrupole ion trap mass spectrometery.
Aplicação
Ethyl 3,3-dimethylacrylate was used in the synthesis of:
- 3-benzylmercupto-3-methylbutanoic acid ethylester
- cis-2-cyano-3,3-dimethylcyclopropanecarboxylic acid, precursor for the synthesis of cis-pyrethroids
- 1-[13CD3]-9-cis-retinoic acid
Palavra indicadora
Warning
Frases de perigo
Classificações de perigo
Flam. Liq. 3
Código de classe de armazenamento
3 - Flammable liquids
Classe de risco de água (WGK)
WGK 2
Ponto de fulgor (°F)
93.2 °F - closed cup
Ponto de fulgor (°C)
34 °C - closed cup
Equipamento de proteção individual
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
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Blank I, et al.
Zeitschrift fur Lebensmittel-Untersuchung Und -Forschung, 195(3), 239-245 (1992)
Synthesis of 1-[13CD3]-9-cis-retinoic acid.
Bennani YL
Journal of Labelled Compounds & Radiopharmaceuticals, 36(8), 755-763 (1995)
Eric Leclerc et al.
Journal of mass spectrometry : JMS, 40(4), 458-463 (2005-02-16)
Ion-molecule reactions between the O=P(OCH3)2 + phosphonium ions and eight alpha,beta-unsaturated esters (methyl acrylate, ethyl acrylate, methyl crotonate, ethyl crotonate, methyl 3,3-dimethylacrylate, ethyl 3,3-dimethylacrylate, methyl methacrylate and ethyl methacrylate) were performed in a quadrupole ion trap mass spectrometer. The O=P(OCH3)2
Taifo Mahmud et al.
The Journal of biological chemistry, 277(36), 32768-32774 (2002-06-27)
Short chain carboxylic acids are well known as the precursors of fatty acid and polyketide biosynthesis. Iso-fatty acids, which are important for the control of membrane fluidity, are formed from branched chain starter units (isovaleryl-CoA and isobutyryl-CoA), which in turn
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