Name | 4-cyclopropylnaphthalen-1-amine |
Synonyms | 4-cyclopropyl-1-naphthalamine 1-phthalemine, 4-cyclopropyl- 4- cyclopropyl-1-naphthylamine 4-cyclopropylnaphthalen-1-amine 4-Cyclopropylnaphthalen-1-aMine 4-Cyclopropyl-1-Naphthalenamine 4-cyclopropyl-1-Naphthalenamine 1-amino-4-cyclopropylnaphthalene 1-naphthalenamine, 4-cyclopropyl- 1-Naphthalenamine, 4-cyclopropyl- 4-Cyclopropyl-1-naphthalenaMine oxalate |
CAS | 878671-94-4 |
EINECS | 200-001-8 |
InChI | InChI=1/C13H13N/c14-13-8-7-10(9-5-6-9)11-3-1-2-4-12(11)13/h1-4,7-9H,5-6,14H2 |
Molecular Formula | C13H13N |
Molar Mass | 183.25 |
Density | 1.191 |
Boling Point | 361.6±21.0 °C(Predicted) |
Flash Point | 190.3°C |
Vapor Presure | 2.04E-05mmHg at 25°C |
pKa | 4.62±0.10(Predicted) |
Storage Condition | Keep in dark place,Inert atmosphere,Room temperature |
Refractive Index | 1.713 |
Use | 4-cyclopropyl-1-naphthylamine is an amine derivative and can be used as an intermediate in organic synthesis. |
preparation | with cheap 1-Naphthylamine as the starting material, protected by amino group, brominated, deprotected by hydrolysis of amino group, 4-cyclopropyl -1-naphthylamine was synthesized by Suzuki method. The synthesis reaction formula is as follows: |