163411. lajstromszámú szabadalom • Eljárás barbitursav-származékok előállítására és e vegyületeket tartalmazó készítmények

163411 /. táblázat Vegyület R1 R2 R3 Z Fizikai állandó száma 1 CH3 CH3 CH3 s 0. p. 86—87 °C 2 CH3 CH3 CH2

CH(CH

3

)

2 s 0. p. 55 °C 3 CH3 CH3 C2

H

5 s 0. p. 76—77 °C 4 CH3 CH3 n-C3

H

7 s 0. p. 66—67 °C 5 CH(CH3

)

2 CH3 CH3 s 0. p. 49 °C 6 C2

H

5 CH3 CH3 s o.p. 72 °C 7 C2

H

5 CH3 C2

H

5 s 0. p. 51 °C 8 CH3 CH3 C6

H

5 s 0. p. 105—106 °C 9 C6

H

5 CH3 CH3 s 0. p. 125 °C 10 CH3 CH3 n-C5

H„ s 0. p. 35 °C 11 CH3 CH3 II-C9H19 s 0. p. 49 °C 12 Cr^CHXC-Hg^ CH3 CH3 s 0. p. 64 °C 13 n-C3

H

7 CH3 CH3 s 0. p. 40 °C 14 n-C4

H

9 CH3 CH3 s 0. p. 64—65 °C 15 C2

H

5 C2

H

5 CH3 s 0. p. 44 °C 16 n-C3

H

7 CH3 C2

H

5 s 0. p. 56 °C 17 C2H5 C2

H

5 C2

H

5 s 0. p. 70—72 °C 18 n-C4

H

9 CH3 C2

H

5 s 0. p. 38 °C 19 n-C3

H

7 CH3 n-C3

H

7 s 0. p. 38 °C 20 n-C4

H

9 CH3 n-C3

H

7 s 0. p. 37 °C 21 C2

H

5 C2

H

5 n-C3

H

7 s 0. p. 28—29 °C 22 n-C4

H

9 CH3 CH2

C

6

Hj s 0. p. 105 °C 23 ciklohexil CH3 CH3 s o.p. 105—107 °C 24 n-C3

H

7 CH3 n-C4

H

9 s 0. p. 43 44 °C 25 n-C4

H

9 CH3 n-C4

H

9 s 0. p. 32—33 °C 26 CH(CH3

)

2 C2

H

5 CH3 s ng 1.5962 27 ciklohexil CH3 n-C3

H

7 s 0. p. 69—70 °C 28 ciklohexil CH3 C2

H

5 s 0. p. 67—68 °C 29 CH3 CH3 n-C4

H

9 s 0. p. 27—28 °C 30 CH2CH = CH2 CH3 CH3 s ng 1.6184 31 C'Jrlo^-'-H ==

^*^2 CH3 n-C3

H

7 s n2

D

3

1.5986 32 n-C3

H

7 CH3 n-C5

H

n s n§ 1.5669 33 n-C5

H„ CH3 CH3 s 0. p. 39—40 °C 34 n-C3

H

7 n-C3

H

7 CH3 s 0. p. 61 °C 35 CH3 CH3 CH(CH3

)

2 s 0. p. 73—74 °C 36 n-C3

H

7 CH3 CH(CH3

)

2 s ng 1.5910 37 C2

H

5 C2

H

5 CH(CH3

)

2 s ng 1.5878 38 CH3 CH3 C(CH3

)

3 s 0. p. 59—60 °C 39 C2

H

5 C2

H

5 n-C4

H

9 s viszkózus olaj 40 n-C3

H

7 C2

H

5 CH3 s 0. p. 54—57 °C 41 C2

H

5 CH3 CH(CH3

)

2 s n^3

1.6055 42 CH2

CH

~ CH2 CH3 C2

H

5 s 0. p. 37—38 °C 43 CH2

CH

= CH2 CH3 n-C4

H

9 s ng1

1.5980 44 CH(CH3

)

2 CH3 C2

H

5 s 0. p. 57—58 °C 45 CH(CH3

))

2 CH3 CH(CH3

)

2 s ng 1.5975 46 CH(CH3

)

2 CH3 n-C4

H

9 s n?3

1.5880 47 CH(CH3

)

2 CH3 n-C3

H

7 s nTM 1.5960 48 CH3 CH3 ciklohexil . s o.p. 111—112 °C 49 C2

H

5 CH3 n-C4

H

9 s 0. p. 32—33 °C 50 n-C5

Hu CH3 n-C3

H

7 s ng 1.5790 51 n-C4

H

9 CH3 CH(CH3

)

2 s ng 1.5843 52 CH(CH3

)

2 C2

H

5 C2

H

5 s ng 1.5962 53 CH(CH3

)

2 C2

H

5 n-C3

H

7 s n^ 1.5879 54 n-C4

H

9 CH3 n-C5

H

u s n2

^

1.5703 55 n-C5

H

u CH3 C2

H

5 s 0. p. 42—43 °C 56 n-C6

H

13 CH3 CH3 s 0. p. 53—55 °C 57 n-C6

H

13 CH3 C2

H

5 s 0. p. 43—44 °C 58 n-C5

H

u CH3 n-C4

H

9 s 0. p. 25 °C 2