Methyl Trans-2-Nonenoate

Product nomen:

Methyl trans-2-nonenoate

Synonyma:

RARECHEM AL BF CLIV, NEOFOLIONE; II-NONENOIC ACIDUM MEthyl ESTER, METHYL NONYLENATE, METHYL NONYLENOATE, Wln: 7U1vo1, METHYL NON II-ENOATE; METHYL-II-NONENATE

CAS;

111-79-5

MF:

C10H18O2

MW:

170.25

EINECS:

203-908-7

Categoria:

Mol fasciculi:

111-79-5.mol

punctum liquescens 

-89.9°C (aestima)

fervens 

115 °C21 mm Hg (lit.)

density 

0.895 g/mL at 25 °C(lit.)

FEMA 

2725 | METHYL 2-NONENOATE

refractivus index 

n20/D 1.444(lit.)

Fp 

196 °F

JECFA Number

1813

CAS Reference

111-79-5 (CAS Reference)

NIST Chemia Reference

Acidum 2-Nonenoicum, yl ester (111-79-5)

EPA Substantia Registry System

Acidum 2-nonenoicum, ester yl (111-79-5)

Periculum Codes 

Petere

Periculum Denunciationes 

36/38-51/53

Salus Denunciationes 

26-61

RIDADR 

UN 3082 9/PG 3

WGK Germania 

2

RTECS 

RA9470000

Descriptio

Methyl 2-nonenoate proprium habet odorem violaceum. Ut habetur in quantitatis cedit tractando yl P-chlorocaproate cum sodium acetate, vel by * dehydrogenating correspondentem saturatum niensis.

Chemical Properties

Methyl-2-nonenoate proprium viridis, hyacinthini odoris

Chemical Properties

Hyalina to flavus liquor fortis violae folium odoris. Stabulum; solutum in alco-hol. Combustible.

Chemical Properties

Methyl 2-Nonenoate pallide lutea liquor viridis hyalinae, nota floralis. dat viriditas in compositionibus floralibus fragrantia commendatur et substituitur for yl 2-octynoate. Synthesis consistit in condensatione heptan cum acido cummalonico, decarboxylatione et subsecutio cum methanolum.

usus

Delibutus.

Praeparatio

nactus in quantitatis cedit, tractando yl β-chlorocaproatum cum sodio acetate; aut dehydrogenating cor [I] respondendo saturatum niensis.

Gustus limina values

Sapor notae ad 5 ppm: viridis, cerae, pinguis, fructuosa, cortice PEPO, pear- et pomum simile.

Nomen commercium

Neofolione (Givaudan).

Rudis materiae

Methanol-->Triethylamine--> acidum Malonicum-->Heptaldehyde-->METHYL NONANOATE