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Merck
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149691

Sigma-Aldrich

Thiazolidine

95%

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About This Item

Fórmula empírica (Notação de Hill):
C3H7NS
Número CAS:
504-78-9
Peso molecular:
89.16
Número CE:
208-002-5
Número MDL:
MFCD00005211
Código UNSPSC:
12352100
ID de substância PubChem:
24848961
NACRES:
NA.22

Ensaio

95%

forma

liquid

índice de refração

n20/D 1.5508 (lit.)

pb

72-75 °C/25 mmHg (lit.)

densidade

1.131 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

C1CSCN1

InChI

1S/C3H7NS/c1-2-5-3-4-1/h4H,1-3H2

chave InChI

OGYGFUAIIOPWQD-UHFFFAOYSA-N

Aplicação

Thiazolidine was used in the synthesis of homogeneous penicillamine disulphide cross-linked polypeptides.

Pictogramas

Flame
GHS02

Palavra indicadora

Warning

Frases de perigo

H226

Classificações de perigo

Flam. Liq. 3

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

132.8 °F - closed cup

Ponto de fulgor (°C)

56 °C - closed cup

Equipamento de proteção individual

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

Certificados de análise (COA)

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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)
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
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
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
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