149691
Thiazolidine
95%
Se connecterpour consulter vos tarifs contractuels et ceux de votre entreprise/organisme
About This Item
Formule empirique (notation de Hill):
C3H7NS
Numéro CAS:
Poids moléculaire :
89.16
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22
Le tarif et la disponibilité ne sont pas disponibles actuellement.
Produits recommandés
Niveau de qualité
Pureté
95%
Forme
liquid
Indice de réfraction
n20/D 1.5508 (lit.)
Point d'ébullition
72-75 °C/25 mmHg (lit.)
Densité
1.131 g/mL at 25 °C (lit.)
Groupe fonctionnel
thioether
Chaîne SMILES
C1CSCN1
InChI
1S/C3H7NS/c1-2-5-3-4-1/h4H,1-3H2
Clé InChI
OGYGFUAIIOPWQD-UHFFFAOYSA-N
Application
Thiazolidine was used in the synthesis of homogeneous penicillamine disulphide cross-linked polypeptides[1].
Mention d'avertissement
Warning
Mentions de danger
Classification des risques
Flam. Liq. 3
Code de la classe de stockage
3 - Flammable liquids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
132.8 °F - closed cup
Point d'éclair (°C)
56 °C - closed cup
Équipement de protection individuelle
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
Faites votre choix parmi les versions les plus récentes :
Déjà en possession de ce produit ?
Retrouvez la documentation relative aux produits que vous avez récemment achetés dans la Bibliothèque de documents.
Les clients ont également consulté
Nampoina Andriamisaina et al.
Phytochemistry, 160, 78-84 (2019-02-12)
The phytochemical study of Ornithogalum dubium Houtt. (Asparagaceae) led to the isolation of five undescribed steroidal glycosides together with two known ones. Their structures were established by using NMR analysis and mass spectrometry as (25R)-3β-hydroxyspirost-5-en-1β-yl O-α-L-arabinopyranosyl-(1 → 2)-α-L-rhamnopyranoside, (25S)-3β-hydroxyspirost-5-en-1β-yl O-β-D-glucopyranosyl-(1 → 6)-β-D-glucopyranoside, (22S)-16β-[(α-L-rhamnopyranosyl)oxy]-22-hydroxycholest-5-en-3β-yl O-β-D-glucopyranosyl-(1 → 4)-β-D-glucopyranoside
Structural analysis of oleanane-type saponins from the roots of Wisteria frutescens.
Anne-Sophie Champy et al.
Magnetic resonance in chemistry : MRC, 55(6), 595-600 (2016-11-20)
Abdelmalek Rezgui et al.
Phytochemistry, 123, 40-47 (2016-01-26)
Four previously undescribed and one known oleanolic acid glycosides were isolated from the roots of Weigela stelzneri, and one previously undescribed and three known hederagenin glycosides were isolated from the leaves. Their structures were elucidated mainly by 2D NMR spectroscopic
Rui-Feng Hu et al.
Chinese journal of natural medicines, 15(6), 436-441 (2017-06-21)
In the present study, 28 Chinese medicinal herbs belonging to traditional Chinese medicine (TCM) for the treatment of type 2 diabetes were selected to explore the application of network pharmacology in developing new Chinese herbal medicine formulae for the treatment
Yasaman Ramazani et al.
Carbohydrate research, 439, 9-15 (2016-12-30)
Cystinosis is a genetic disorder caused by malfunction of cystinosin and is characterized by accumulation of cystine. Cysteamine, the medication used in cystinosis, causes halitosis resulting in poor patient compliance. Halitosis is mainly caused by the formation of dimethylsulfide as
Active Filters
Notre équipe de scientifiques dispose d'une expérience dans tous les secteurs de la recherche, notamment en sciences de la vie, science des matériaux, synthèse chimique, chromatographie, analyse et dans de nombreux autres domaines..
Contacter notre Service technique
