cas 1430230-65-1|| where to buy tert-butyl N-[trans-4-hydroxyoxolan-3-yl]carbamate

Nom du produit:tert-butyl N-[trans-4-hydroxyoxolan-3-yl]carbamate

IUPAC Name:tert-butyl N-[(3R,4S)-4-hydroxyoxolan-3-yl]carbamate

Unité d'emballage	Stock disponible	Prix($)
CM104608-1g	in stock	źƞ
CM104608-5g	in stock	ȎĽŉ

Pour une utilisation en R&D uniquement..

Formulaire de demande

Nom chimique

Numéro CAS

Quantité*

Spécifications requises*
(% d'analyse, qualité du matériau, etc.)

Nom du contact*

Email du contact*

Meanwhile I'd like to create a registered account on CHEMENU.COM with the above email.

I'd like to receive emails related to products with similar structures to 1430230-65-1 regularly via the above email.

Notes supplémentaires

Verification code*

refresh

: N° CAS:1430230-65-1; Formule moléculaire:C9H17NO4; Point de fusion:-; Code SMILES:CC(C)(C)OC(=O)N[C@@H]1COC[C@H]1O; Densité:

: Numéro de catalogue:CM104608; Poids moléculaire:203.24; Point d'ébullition:; N° Mdl:; Stockage:

: Tetrahydrofurans; Tetrahydrofuran is a heterocyclic organic compound with the molecular formula C4H8O. Tetrahydrofuran belongs to ethers and is the complete hydrogenation product of furan. It is a colorless, water-miscible organic liquid with small viscosity at normal temperature and pressure. Because of its long liquid range, it is a commonly used medium polar aprotic solvent. Its main use is as a precursor of high molecular polymers.

: Furans; Furan is a cyclic flammable liquid compound C4H4O that is obtained from wood oils of pines or made synthetically and is used especially in organic synthesis. Furan is aromatic because a pair of lone pair electrons of the oxygen atom in its molecule forms a large π bond in the plane of the conjugated orbital, making a total of 6 electrons in the plane of the conjugated plane, conforming to the 4n+2 structure. Aromaticity makes furan have the property of easy substitution and difficult addition. The other lone pair of electrons in oxygen stretches out. The oxygen atom itself conforms to sp2 hybridization. Due to the presence of the aromatic ring, the chemical behavior of furan is not very similar to that of other unsaturated heterocycles. The oxygen in the aromatic ring has an electron-donating effect, so the electrophilic substitution reactivity of furan is stronger than that of benzene.