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Crotonic acid, -, ethyl ester

Chromium trioxide, 60, 21 Clemmensen reaction, 60, 111 Copper chloride (CuCl) [7758-89-6], 61, 122 Crotonic acid, ethyl ester, ( )-, 61, 85 18-Crown-6-potassium cyanide complex, 60,129 Crum Brown-Walker reaction, 60, 4 Cuprous chloride, 60, 42, 121 61, 122 CYANIC ACID, PHENYL ESTER [1122-85-6], 61, 35... [Pg.80]

Ethyl crotonate Crotonic acid, ethyl ester, (E)- (8) 2-Butenoic acid, ethyl ester, ( )- (9) (623-70-1)... [Pg.136]

SYNS 2-BUTENOIC ACID, ETHYL ESTER CROTONIC ACID, ETHYL ESTER ETHYLESTER KYSEUNY KROTONOVE... [Pg.616]

UN 1862 (DOT) FEMA 3486 Synonyms 2-Butenoic acid, ethyl ester trans-2-Butenoic acid ethyl ester Crotonic acid, ethyl ester Ethyl trans-2-butenoate Ethyl a-crotonate... [Pg.1699]

CgHsBrOi 4-bromo-tra s-crotonic acid ethyl ester 37746-78-4... [Pg.137]

C6H9CIO2 2-chloro-fra s-crotonic acid ethyl ester 77825-54-8 ... [Pg.138]

C6H9CIO2 3-chloro-cis-crotonic acid ethyl ester 6127-92-0 ... [Pg.138]

SYNS 2-BUTENOIC ACID, ETHYL ESTER, (E)-(9CI) orans-2-BUTENOIC ACID ETHYL ESTER CROTONATE d ETHYLE (FRENCH) ETHYL (E)-2-BUTENOATE ETHYLCROTONATE ETHYL (E)-CROTONATE ETHYL trans-CROTONATE ETHYL CROTONATE (DOT)... [Pg.393]

Butenoic acid, butyl ester (E)-2-Butenoic acid butyl ester. See Butyl crotonate 2-Butenoic acid, 4,4 -((dibutylstannylene) bis (oxy)) bis (4-oxo)-, diisooctyl ester, (Z,Z)-. See Dibutyltin diisooctylmaleate 2-Butenoic acid, ethyl ester trans-2-Butenoic acid ethyl ester. See Ethyl crotonate 2-Butenoic acid, hexyl ester. See Hexyl 2-butenoate... [Pg.588]

Partially saponified poly(vinyl acetate) Fully saponified poly(vinyl acetate) Copolymers with crotonic acid Copolymers with vinyl acetate with methacrylic acid with acrylic acid esters with acrylonitrile with styrene with ethyl vinyl ether with butadiene... [Pg.97]

Figure 11.11 Pyrogram of a paint sample collected from a decorative frame of the Universal Judgement by Bonamico Buffalmacco (fourteenth century, Monumental Cemetery of Pisa, Italy). Pyrolysis was performed with a microfurnace pyrolyser, at 600°C, in the presence of HMDS. 1, Benzene 2, ethyl acrylate 3, methyl methacrylate 4, acetic acid, trimethyl silyl ester 5, pyrrole 6, toluene 7, 2 methylpyrrole 8, 3 methylpyrrole 9, crotonic acid 10, ben zaldehyde 11, phenol 12, 2 methylphenol 13, 4 methylphenol 14, 2,4 dimethyl phenol 15, benzyl nitrile 16, 3 phenylpropionitrile 17, indole 18, phthalate 19, phthalate 20, ben zyl benzoate HMDS pyrolysis products [27]... Figure 11.11 Pyrogram of a paint sample collected from a decorative frame of the Universal Judgement by Bonamico Buffalmacco (fourteenth century, Monumental Cemetery of Pisa, Italy). Pyrolysis was performed with a microfurnace pyrolyser, at 600°C, in the presence of HMDS. 1, Benzene 2, ethyl acrylate 3, methyl methacrylate 4, acetic acid, trimethyl silyl ester 5, pyrrole 6, toluene 7, 2 methylpyrrole 8, 3 methylpyrrole 9, crotonic acid 10, ben zaldehyde 11, phenol 12, 2 methylphenol 13, 4 methylphenol 14, 2,4 dimethyl phenol 15, benzyl nitrile 16, 3 phenylpropionitrile 17, indole 18, phthalate 19, phthalate 20, ben zyl benzoate HMDS pyrolysis products [27]...
Homologation of a,fl-umatwrated carboxylic acids. Ethyl crotonate can be alkylated at C3 by CuCl-catalyzed addition of Grignard reagents followed by treatment with methanesulfinyl chloride. Subsequent desulfinylation yields the homologated unsaturated ester (equation I). The method is also applicable to a,/ -enones (equation II).10... [Pg.129]

These materials are the reaction product of a primary amine and either acrylic acid, an ester of acrylic acid such as methyl acrylate, ethyl acrylate or crotonic acid. Either 1 or 2 mol of acrylate is used. If 1 mol is added, an N-alkyl (3-alanine is produced (Figure 6.6) and if 2 mol of acrylate per mole of amine is used, the corresponding carboxyethyl (3 -alanine derivative is produced (Figure 6.7). [Pg.170]

The results obtained for the asymmetric 1,4-addition of arylboionic acids to crotonates or cinnamates in the presence of a Rh(acac)(C2H4)2-(S)-binap catalyst are summarized in Table 3. The ester group (R2) significantly affects the %ee. Thus, the i-propyl, cyclohexyl, (-butyl, benzyl esters achieved a high %ee whereas the methyl and ethyl esters (entries 1-4) resulted in low asymmetric induction. The absolute configuration of benzyl 3-phenylbutanoate ([a]D -14.5 (c 1.02, CHC13) obtained from (S)-binap was established to be (R) by the specific rotation reported for (R)-3-phenylbutanoic acid ([a]D -45.8 (c 0.77, benzene). [Pg.403]

ETHYL P-ANILINOCROTONATE (Crotonic acid, P-anilino-, ethyl ester)... [Pg.42]

Pudovik, A.N., Addition of dialkyl phosphites to unsaturated compounds. Part 6. Addition of dialkyl phosphites to ethyl esters of cinnamic and crotonic acids. Zh. Obshch. Khim.. 22. 1143. 1952 Chem. Abstr, 47, 4836h, 1953. [Pg.502]

See other pages where Crotonic acid, -, ethyl ester is mentioned: [Pg.393]    [Pg.1596]    [Pg.71]    [Pg.1099]    [Pg.1100]    [Pg.393]    [Pg.1596]    [Pg.71]    [Pg.1099]    [Pg.1100]    [Pg.1648]    [Pg.127]    [Pg.112]    [Pg.113]    [Pg.105]    [Pg.54]    [Pg.24]    [Pg.24]    [Pg.527]   
See also in sourсe #XX -- [ Pg.61 , Pg.85 ]



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Croton

Crotonate

Crotonates

Crotonic

Crotonic 3- -, ethyl ester

Crotonic acid

Crotonization

Trans-Crotonic acid ethyl ester

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