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同位素純度
99.8 atom % D
化驗
99% (CP)
形狀
liquid
包含
1 % (v/v) TMS
技術
NMR: suitable
雜質
≤0.0100% water
water
折射率
n20/D 1.444 (lit.)
bp
60.9 °C (lit.)
mp
−64 °C (lit.)
密度
1.500 g/mL at 25 °C (lit.)
質量偏移
M+1
SMILES 字串
[2H]C(Cl)(Cl)Cl
InChI
1S/CHCl3/c2-1(3)4/h1H/i1D
InChI 密鑰
HEDRZPFGACZZDS-MICDWDOJSA-N
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一般說明
氯仿-d（氘代氯仿，CDCl 3 ）是氯仿的氘代衍生物。含有 1% (v/v) TMS（四甲基硅烷，作为稳定剂加入）。本文报道了氯仿-d 在不同有机溶剂中的碳氘伸缩峰的定量红外光谱研究。 用 Raman 差谱研究了氯仿-d 和液体氯仿混合物在 cCHCl3 和 CDCl3 的1 和 2 谱带中的频移。
應用
氯仿-d 已被用作氘代溶剂，用于含 α-苯乙基的 β-氨基丙酸相应手性衍生物的 NMR 谱研究，它们可作为 β-氨基酸不对称合成的有用起始原料。
推薦產品
訊號詞
Danger
危險分類
Acute Tox. 3 Inhalation - Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Repr. 2 - Skin Irrit. 2 - STOT RE 1 Oral - STOT SE 3
標靶器官
Liver,Kidney, Respiratory system
儲存類別代碼
6.1D - Non-combustible acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects
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
Eyeshields, Faceshields, Gloves
Preparation of chiral derivatives of ?-Ala containing the a-phenylethyl group: useful starting materials for the asymmetric synthesis of ?-amino acids
Guzman-Mejia R, et al.
Nature Protocols, 2(11), 2759-2766 (2007)
Isotopic dilution studies of the chloroform-chloroform-d system by Raman difference spectroscopy.
Laane J and Kiefer W.
J. Chem. Phys. , 73(10), 4971-4975 (1980)
Quantitative Study of the Bonding of Chloroform-d in Various Solvents by Infrared Spectrometry1.
Lord RC, et al.
Journal of the American Chemical Society, 77(5), 1365-1368 (1955)
Ramón Guzmán-Mejía et al.
Nature protocols, 2(11), 2759-2766 (2007-11-17)
The use of microwave (MW) irradiation for the condensation reaction between acetophenone and alpha-phenylethylamine to prepare (R,R)-bis[alpha-phenylethyl]amine results in significantly reduced reaction times relative to the use of conventional heating. In this protocol, a secondary amine, (R,R)-bis(alpha-phenylethyl)amine is treated with
Chong Li et al.
Nature communications, 5, 5709-5709 (2014-12-17)
Photoswitchable fluorescent diarylethenes are promising in molecular optical memory and photonic devices. However, the performance of current diarylethenes is far from satisfactory because of the scarcity of high-speed switching capability and large fluorescence on-off ratio. Here we report a trident
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