Consentement d'utilisation des Cookies

J'accepte Notre site sauvegarde des traceurs textes (cookies) sur votre appareil afin de vous garantir de meilleurs contenus et à des fins de collectes statistiques.Vous pouvez désactiver l'usage des cookies en changeant les paramètres de votre navigateur. En poursuivant votre navigation sur notre site sans changer vos paramètres de navigateur vous nous accordez la permission de conserver des informations sur votre appareil.

33884-43-4 - 2-(2-Bromoethyl)-1,3-dioxane, 98% - 2-Bromopropanal 1,3-propanediol acetal - 2-Bromopropionaldehyde trimethylene acetal - L00958 - Alfa Aesar

L00958 2-(2-Bromoethyl)-1,3-dioxane, 98%

Numéro CAS
33884-43-4
Synonymes
2-Bromopropanal 1,3-propanediol acetal
2-Bromopropionaldehyde trimethylene acetal

Dimensions Prix ($) Quantité Disponibilité
10g 26,10
50g 88,90
Ajouter au panier Ajouter au devis en vrac Afficher l'article

2-(2-Bromoethyl)-1,3-dioxane, 98%

MDL
MFCD00006567
EINECS
251-716-7

Propriétés chimiques

Formule
C6H11BrO2
Poids formulaire
195.06
Point d'ébullition
67-70°/3mm
Point d'éclair
96°(204°F)
Densité
1.434
Indice de réfraction
1.4820
Solubilité
It is not soluble in water but soluble in organic solvent such as ethanol.

Applications

2-(2-Bromoethyl)-1,3-dioxane, Provides a useful means of introducing a masked ß-formylethyl group. In comparison with the corresponding dioxolane (following entry), the dioxane is more stable to acid, and the Grignard is thermally stable. Reaction of the Grignard with an acid chloride gives the ketone in high yield without further reaction to the tertiary alcohol. Subsequent hydrolysis of the 1,3-dioxane gives the -ketoaldehyde. It is also used as a pharmaceutical intermediate.

Notes

Air, Heat sensitive. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from oxidizing agents. Stable under recommended storage conditions.

Références bibliographiques

JC Stowell. New. gamma.-keto Aldehyde synthesis. The Journal of Organic Chemistry. 197641(3) , 560-561.

A Fadel.; P Arzel. Asymmetric construction of benzylic quaternary carbons by lipase-mediated enantioselective transesterification of prochiral α, α-disubstituted 1, 3-propanediols. Tetrahedron: Asymmetry. 19978(2) , 283-291.

Provides a useful means of introducing a masked ß-formylethyl group. In comparison with the corresponding dioxolane (following entry), the dioxane is more stable to acid, and the Grignard is thermally stable. Reaction of the Grignard with an acid chloride gives the ketone in high yield without further reaction to the tertiary alcohol. Subsequent hydrolysis of the 1,3-dioxane gives the -ketoaldehyde: J. Org. Chem., 41, 560 (1976).

Mentions de danger et de prudence du SGH

Mentions de danger (UE): H315-H319-H335

Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.

Mentions de prudence: P260u-P201-P280a-P303+P361+P353-P305+P351+P338-P301+P330+P331-P304+P340-P310a-P405-P501a

Obtain special instructions before use. Wear protective gloves and eye/face protection. IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. IF INHALED: Remove to fresh air and keep at rest in a position comfortable for breathing. Store locked up. Dispose of contents/container in accordance with local/regional/national/international regulations.

Autres références

Beilstein
1421628
Code tarifaire harmonisé
2932.99
TSCA
Yes

Recommandé

Consulté récemment

Produits chimiques

Sciences de la vie

Métaux et matériaux

Catalyseurs

Analytique et matériel de laboratoire