Schmelzpunkttabellen Organischer Verbindungen / Melting by Dr. Walther Utermark, Dr. Walter Schicke (auth.)

By Dr. Walther Utermark, Dr. Walter Schicke (auth.)

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Extra resources for Schmelzpunkttabellen Organischer Verbindungen / Melting Point Tables of Organic Compounds / Tableaux des Points de Fusion des Composés Organiques / Тoчки Плaвления Органическиx Соединениӥ

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31 -127,0 Buten-(2) C4H s CH a· CH: CH· CH 3 56,10 Gas 42,08 Gas 98,18 FI. 32 (ß-Butylen) -127,0 Cyclopropan (Trimethylen) CaH 6 33 -126,4 Methylcyclohexan C7H 14 / CH 2 • CH 2 ' " H 2C '" / CH· CH 3 CH 2 ·CH2 34 -126,0 n-Propylalkohol CaHsO C2 H 5 ·CH2 OH 60,09 FI. 35 -124,8 ß- Brompropen CaH 5 Br CH 3 ·CBr:CH2 120,99 FI. 36 -124,0 Trimethylamin C3 H 9N (CH3 laN 59,11 Gas H 2C '" I /CH2 H 2C 7 -130,8 bis -124,0 Lfd. Spez. Nr. ) 1436 31 0,6315 32 1. + 1,0 2. +2,5 0,720 -34,5 (75Omm) 1204 V 15 33 0,7718170 100,3 V29 34 0,8044200 97,2 24,83 (20mm) 19,04 (14mm) 1350 35 13,965 48,4 1200 36 0,662-50 -3,5 IV 43 Physikalische Konstanten und Eigenschaften Löslichkeit Reaktionen 11 12 13 nD2°1,35800; RD20 25,28 cms ; nF2°61,9; Dampfdruck 20° 422 mm Hg nD I6 1,41152; RD16 16,95 cms ; nF16 96,6; heftig reizender Geruch; giftig 2 stereoisomere Formen wird von H 2SO, absorbiert uni.

162 -70,0 Diisobutylamin CsH 19N [(CHS)2CH. CH 2]2NH 129,24 Fl. C4 H sCIS HC-CH 118,59 Fl. 163 isopropylbenzol) säureanhydrid ) (Tri) -70 bis 2-Chlorthiophen 11 11 -69 HC C·CI ~/ S 164 -69,9 (X-Picolin ((X-Methylpyridin) Fl. C6H 7N ()-CHs N 35 -73,9 bis -69,9 Ud. Spez. Nr. 14,39 (20mm) 11240 157 0,8586200 176,7 70,3 (20mm) V 420 nDIS,? 1,4926; unI. in W RDI3,? 45,18-cm3; 1. in A, Ae nF13,? 140,0; Dampfdruck 40° 38mmHg; ebullioskop. Konst. 5,34; riecht möhrenähnlich, eigentüml. herb + H 2SO, ~ orange 158 1,082200 139,4 49,1 (20mm) 11 166 Kochen mit krist.

Aggregatzustand GeFarbe wicht 6 7 68,03 Gas 63 -111,3 Kohlensuboxyd C30 2 O:C:C:C:O 64 -110,9 Athyljodid C2H 5J C2H 5J 155,98 FI. 65 -110,8 3-Fluortoluol C7H 7F F·C6 H 4 ·CH3 110,13 FI. FI. 67 -108,0 Isobutylalkohol (Isopropylcarbinol) C,HlOO (CH3)2CH· CH 20H 74,12 FI. -Amylamin C5 H 13N CzH 5 ' C(CH3)2' NH 2 87,16 FI. 76,16 FI. 69 -100,0 Methyläthylsulfid C3H sS CH 3·S·C2H 5 70 -100,0 Formaldehyddimethylacetal (Methylal) C3H s0 2 CH 30· CH 2 • OCH 3 76,09 FI. -Butyljodid C4H 9 J C2H 5 • CHJ .

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