推薦產品
蒸汽密度
2.43 (vs air)
蒸汽壓力
635 psi ( 21 °C)
化驗
≥98%
bp
−84 °C (lit.)
mp
−160 °C (lit.)
SMILES 字串
FC(F)F
InChI
1S/CHF3/c2-1(3)4/h1H
InChI 密鑰
XPDWGBQVDMORPB-UHFFFAOYSA-N
包裝
Supplied in a carbon steel lecture bottle with a CGA180M/CGA110F needle valve installed.
Compatible with the following:
Compatible with the following:
- Aldrich® lecture-bottle station systems
- Aldrich® lecture-bottle gas regulators
其他說明
See Technical Information Bulletin AL-151 Gas Regulators: Selection, Installation, and Operation
法律資訊
Aldrich is a registered trademark of Sigma-Aldrich Co. LLC
也與該產品經常一起購買
產品號碼
描述
訂價
排氣閥
控制閥
推薦
產品號碼
描述
訂價
校準器
訊號詞
Warning
危險聲明
防範說明
危險分類
Press. Gas Liquefied gas
儲存類別代碼
2A - Gases
水污染物質分類（WGK）
WGK 1
閃點（°F）
Not applicable
閃點（°C）
Not applicable
個人防護裝備
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
Naleen B Jayaratna et al.
Inorganic chemistry, 52(4), 1691-1693 (2013-02-02)
Silver and copper ethylene adducts and the silver carbonyl complex of the tris(pyrazolyl)borate [HB(3,4,5-(CF(3))(3)Pz)(3)](-) (which is based on one of the most acidic pyrazoles known) have been synthesized. (13)C NMR resonance signals of metal-bound ethylene carbon atoms of [HB(3,4,5-(CF(3))(3)Pz)(3)]Ag(C(2)H(4)) and
Alessandro Zanardi et al.
Journal of the American Chemical Society, 133(51), 20901-20913 (2011-12-06)
We have found the first reaction of direct cupration of fluoroform, the most attractive CF(3) source for the introduction of the trifluoromethyl group into organic molecules. Treatment of CuX (X = Cl, Br, I) with 2 equiv of MOR (M
Sven P Fritz et al.
Organic letters, 14(24), 6370-6373 (2012-12-13)
CF(3)-substituted vinyl diphenylsulfonium triflate is an effective annulation reagent for the formation of α-CF(3) substituted, epoxide-fused heterocycles (pyrrolidines, piperidines, and tetrahydrofurans). This simple method affords a variety of valuable heterocyclic building blocks in a highly diastereoselective manner (dr >20:1).
Naeem Iqbal et al.
The Journal of organic chemistry, 77(24), 11383-11387 (2012-11-22)
A method for trifluoromethylation of alkenes has been developed employing visible light photoredox catalysis with CF(3)I, Ru(Phen)(3)Cl(2), and DBU. This process works especially well for terminal alkenes to give alkenyl-CF(3) products with only E-stereochemistry. The mild reaction conditions enable the
Nicolas Susperregui et al.
The Journal of organic chemistry, 75(19), 6581-6587 (2010-08-31)
The mechanism of ring-opening of ε-caprolactone by methanol catalyzed by trifluoromethane and methane sulfonic acids has been studied computationally at the DFT level of theory. For both elementary steps, the sulfonic acid was predicted to behave as a bifunctional catalyst.
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