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Merck
CN

149691

四氢噻唑

95%

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关于此项目

经验公式(希尔记法):
C3H7NS
化学文摘社编号:
分子量:
89.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
208-002-5
MDL number:
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产品名称

四氢噻唑, 95%

InChI key

OGYGFUAIIOPWQD-UHFFFAOYSA-N

InChI

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

SMILES string

C1CSCN1

assay

95%

form

liquid

refractive index

n20/D 1.5508 (lit.)

bp

72-75 °C/25 mmHg (lit.)

density

1.131 g/mL at 25 °C (lit.)

functional group

thioether

Quality Level

Application

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

pictograms

Flame

signalword

Warning

hcodes

Hazard Classifications

Flam. Liq. 3

存储类别

3 - Flammable liquids

wgk

WGK 3

flash_point_f

132.8 °F - closed cup

flash_point_c

56 °C - closed cup

ppe

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

法规信息

危险化学品
此项目有

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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
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)
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

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