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Merck

235253

Sigma-Aldrich

二乙胺基三氟化硫

95%

别名:

DAST, 二乙氨基三氟化硫

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About This Item

线性分子式:
(C2H5)2NSF3
CAS号:
分子量:
161.19
Beilstein:
1849066
EC號碼:
MDL號碼:
分類程式碼代碼:
12352101
PubChem物質ID:
NACRES:
NA.22

品質等級

化驗

95%

形狀

liquid

bp

30-32 °C/3 mmHg (lit.)

密度

1.22 g/mL at 25 °C (lit.)

儲存溫度

2-8°C

SMILES 字串

CCN(CC)S(F)(F)F

InChI

1S/C4H10F3NS/c1-3-8(4-2)9(5,6)7/h3-4H2,1-2H3

InChI 密鑰

CSJLBAMHHLJAAS-UHFFFAOYSA-N

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一般說明

二乙氨基三氟化硫(DAST)是一种氟化试剂,用于合成含氟化合物和开环反应。

應用

  • 氟化剂:与醇和羰基化合物反应,综述
  • 关于亲核氟化的综述。
  • 在使用叔环丙基甲硅烷基醚进行Friedel-Crafts烯丙基化 和均聚醇重排成不饱和醛过程中的催化剂。
  • 在26-氟-埃坡霉素的合成中,氟甲基的早期引入可在进一步的操作过程中稳定环氧化物。
  • 可用于多种化合物(包括硫醚、链烯醇和氰醇)的氟化剂。
  • 用于酮基哌啶酸的宝石二氟化试剂。

取代透過

产品编号
说明
价格

象形圖

FlameCorrosion

訊號詞

Danger

危險聲明

危險分類

Eye Dam. 1 - Flam. Liq. 3 - Self-react. D - Skin Corr. 1A

安全危害

儲存類別代碼

5.2 - Organic peroxides and self-reacting hazardous materials

水污染物質分類(WGK)

WGK 3

閃點(°F)

73.4 °F

閃點(°C)

23 °C

個人防護裝備

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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Recent advances in nucleophilic fluorination reactions of organic compounds using Deoxofluor and DAST
RP Singh, et al.
Synthesis, 2002, 2561-2578 (2002)
Jindřich Karban et al.
Organic & biomolecular chemistry, 10(2), 394-403 (2011-11-16)
A complete series of eight 1,6:2,3- and 1,6:3,4-dianhydro-β-D-hexopyranoses were subjected to fluorination with DAST. The 1,6:3,4-dianhydropyranoses yielded solely products of skeletal rearrangement resulting from migration of the tetrahydropyran oxygen (educts of D-altro and D-talo configuration) or of the 1,6-anhydro bridge
Reaction of tertiary cyclopropyl silyl ethers with diethylaminosulfur trifluoride. Part 2: The Friedel-Crafts allylation and cyclopropylation of electron-rich aromatic compounds
Kirihara, Masayuki, et al.
Tetrahedron Letters, 47, 3777-3777 (2006)
Aurélien Bigot et al.
Organic letters, 13(2), 192-195 (2010-12-15)
The design of a new potent nonsteroidal ecdysone agonist led to the discovery of a diethylaminosulfur trifluoride (DAST)-mediated cyclization of α,α-disubstituted-α-acylaminoketones. The resulting fluorooxazolines can be ring-opened or selectively substituted by a range of nucleophiles to provide in high yields
P G Hultin et al.
Carbohydrate research, 322(1-2), 14-25 (2000-01-12)
We have made thioglycoside donors for the 4,6-dideoxy-L-lyxo-hexopyranosyl ('4-deoxy-L-rhamnosyl') and 4-deoxy-4-fluoro-L-rhamnosyl monosaccharide residues. The preparation of the deoxyfluororhamnose was not straightforward, and revealed some unexpected behavior of the diethylaminosulfur trifluoride (DAST) reagent. The new glycosyl donors were used to synthesize

商品

Diethylaminosulfur trifluoride (DAST) facilitates nucleophilic fluorination in selective reactions with alcohols, ketones, and other compounds.

Diethylaminosulfur trifluoride (DAST) facilitates nucleophilic fluorination in selective reactions with alcohols, ketones, and other compounds.

Diethylaminosulfur trifluoride (DAST) facilitates nucleophilic fluorination in selective reactions with alcohols, ketones, and other compounds.

Diethylaminosulfur trifluoride (DAST) facilitates nucleophilic fluorination in selective reactions with alcohols, ketones, and other compounds.

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