4-Aminobenzoic acid methyl ester

Aminobenzoic acid methyl ester 2295A I(3)1371A, N(2)284A CB3325000... [Pg.1051]

Methyl anthranilate (2-aminobenzoic acid methyl ester)... [Pg.16]

SYNS o-AMINOBENZOIC ACID METHYL ESTER 2-AMINOBENZOIC ACID METHYL ESTER o-CARBOMETHOXYANILINE 2-CARBOMETHO-XYANILINE FEMA No. 2682 2-(METHOXY-CARBONYL)ANILINE METHYL o-AIvIINOBENZO-ATE METHYL 2-AMINOBENZOATE METHYL ANTHRANILATE (FCC) METHYLESTER KYSELINY ANTHRANILOVE NEROLI OIL, ARTIFICAL... [Pg.89]

Aminobenzoic acid methyl ester o-Aminobenzoic acid methyl ester. See Methyl anthranilate... [Pg.215]

Synonyms 2-Aminobenzoic acid methyl ester o-Aminobenzoic acid methyl ester Anthranilic acid methyl ester Benzoic acid, 2-amino-, methyl ester 2-Carbomethoxyaniline o-Carbomethoxyaniline 2-(Methoxycarbonyl) aniline Methyl 2-ami nobenzoate Methyl-o-aminobenzoate Methyl 2-anthranilate Neroli oil, artificial... [Pg.2585]

Aminobenzoic acid methyl ester, L 2.45 0.05 -5.1 -6 48KH,67CW... [Pg.333]

Aminobenzoic acid methyl ester HL/H.L (CyHy02N), L (Other references in Vol.2, p.333)... [Pg.471]

P.22) Benzoic acid, 2-amino-, methyl ester, methyl anthranilate, methyl 2-aminobenzoate, anthranilic acid methyl ester [134-20-3] FEMA 2682... [Pg.333]

Synonyms cas 94-14-4 p-aminobenzoic acid isobutyl ester (2-methyl)-p-aminobenzoate Isobutylene-Isoprene Copolymer... [Pg.176]

The reaction of 2-aminobenzoic acid hydrazidcs with ortho esters gives 4-methyl-3//-1,3,4-benzotriazepin-5(4//)-ones 17 or 4-methyl-l//-l, 3,4-benzotriazepin-5(4//)-ones 18, depending on the structure of the hydrazide. Selected examples are given.359 11 360 361... [Pg.466]

Ethyl p-aminobenzoate (esterification of p-aminobenzoic acid). Place 80ml of absolute ethanol in a 250-ml two-necked flask equipped with a double surface reflux condenser and a gas inlet tube. Pass dry hydrogen chloride (Section 4.2.38, p. 438) through the alcohol until saturated - the increase in weight is about 20 g - remove the gas inlet tube, introduce 12 g (0.088 mol) of p-aminobenzoic acid and heat the mixture under reflux for 2 hours. Upon cooling, the reaction mixture sets to a solid mass of the hydrochloride of ethyl p-aminobenzoate. It is better, however, to pour the hot solution into c. 300 ml of water (no hydrochloride separates) and add solid sodium carbonate carefully to the clear solution until it is neutral to litmus. Filter off the precipitated ester at the pump and dry in the air. The yield of ethyl p-aminobenzoate, m.p. 91 °C, is 10 g (69%). Recrystallisation from rectified (or methylated) spirit does not affect the m.p. [Pg.897]

Raney nickel) of the potassium salt of D-xy/o-5-hexulosonic acid oxime produces a mixture of 5-amino-5-deoxy-L-idonic and -D-glu-conic acid in the ratio of 2 1, which is converted into the methyl ester hydrochloride. Upon treatment with alkali, spontaneous cyclization to the pair of 1,5-lactams occurs. 5-Amino-5-deoxy-L-idono-l,5-lactam and 5-amino-5-deoxy-D-glucono-l,5-lactam were separated by recrystallization. The optical rotatory dispersion curves of both compounds were discussed. A new type of lactam, namely, 2-enamino-N,N -bis[(p-methoxycarbonyl)phenyl]-4-(D-gaiacfo-penta-acetoxypentyl)-4-butanelactam was prepared by tbe reaction of 5,6,7,8,9-penta-0-acetyl-3,4-dideoxy-D-ga/ocfo-nonulos- rcns-3-en-l-onic acid with methyl p-aminobenzoate. [Pg.166]

Some relationships between the dipole moment and molecular structure have also been found in the case of aliphatic compounds. In the first instance we may mention the two methyl esters of a- and 8-aminovaleric acid. We should expect from the results for the aminobenzoic acids that in an open chain the moment of the 8-ester would be greater than that of the a-ester, while in a chain joined into a ring the moments should be about the same. The values obtained... [Pg.32]

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