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Merck

149691

Sigma-Aldrich

四氢噻唑

95%

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1 G
$91.30
5 G
$183.00

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1 G
$91.30
5 G
$183.00

About This Item

经验公式(希尔记法):
C3H7NS
CAS号:
分子量:
89.16
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22
形狀:
liquid
化驗:
95%

$91.30


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品質等級

化驗

95%

形狀

liquid

折射率

n20/D 1.5508 (lit.)

bp

72-75 °C/25 mmHg (lit.)

密度

1.131 g/mL at 25 °C (lit.)

官能基

thioether

SMILES 字串

C1CSCN1

InChI

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

InChI 密鑰

OGYGFUAIIOPWQD-UHFFFAOYSA-N

應用

Thiazolidine was used in the synthesis of homogeneous penicillamine disulphide cross-linked polypeptides[1].

象形圖

Flame

訊號詞

Warning

危險聲明

危險分類

Flam. Liq. 3

儲存類別代碼

3 - Flammable liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

132.8 °F - closed cup

閃點(°C)

56 °C - closed cup

個人防護裝備

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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)
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
Mayra Rengifo Carrillo et al.
Phytochemistry, 140, 166-173 (2017-05-14)
The phytochemical study of two cultivars of Pittosporum tenuifolium Banks & Sol. ex Gaertn, "variegatum" and "gold star", led to the isolation of eight oleanane-type glycosides: seven previously undescribed and a known one. Their aglycons are oxygenated oleanane derivatives as
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
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

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