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Merck

483877

Sigma-Aldrich

5-(三氟甲基)二苯并噻吩三氟甲磺酸盐

97%

别名:

S-(三氟甲基)二苯并噻吩三氟甲磺酸盐

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About This Item

经验公式(希尔记法):
C14H8F6O3S2
分子量:
402.33
MDL號碼:
分類程式碼代碼:
12352101
PubChem物質ID:
NACRES:
NA.22

化驗

97%

mp

150 °C (lit.)

SMILES 字串

[O-]S(=O)(=O)C(F)(F)F.FC(F)(F)[S+]1c2ccccc2-c3ccccc13

InChI

1S/C13H8F3S.CHF3O3S/c14-13(15,16)17-11-7-3-1-5-9(11)10-6-2-4-8-12(10)17;2-1(3,4)8(5,6)7/h1-8H;(H,5,6,7)/q+1;/p-1

InChI 密鑰

QXXHXTRTGZBOGD-UHFFFAOYSA-M

應用

  • Pd(II)-催化的三氟甲基化
  • 离子液体中的亲电子三氟甲基化
  • 使用Umemoto试剂和铜催化剂通过末端炔烃的三氟甲基化立体选择性制备三氟甲基炔烃

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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Tetrahedron Letters, 53, 2769-2772 (2012)
Jun Xu et al.
Journal of the American Chemical Society, 133(39), 15300-15303 (2011-09-15)
An unprecedented type of reaction for Cu-catalyzed trifluoromethylation of terminal alkenes is reported. This reaction represents a rare instance of catalytic trifluoromethylation through C(sp(3))-H activation. It also provides a mechanistically unique example of Cu-catalyzed allylic C-H activation/functionalization. Both experimental and
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Journal of the American Chemical Society, 134(29), 11948-11951 (2012-07-12)
A Pd(II)-catalyzed trifluoromethylation of ortho C-H bonds with an array of N-arylbenzamides derived from benzoic acids is reported. N-Methylformamide has been identified as a crucial promoter of C-CF(3) bond formation from the Pd center. X-ray characterization of the C-H insertion

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