推荐产品
等級
SAJ first grade
蒸汽密度
9.25 (vs air)
化驗
≥98.0%
形狀
liquid
存貨情形
available only in Japan
bp
67-69 °C/11 mmHg (lit.)
mp
5-8 °C (lit.)
密度
3.325 g/mL at 25 °C (lit.)
SMILES 字串
ICI
InChI
1S/CH2I2/c2-1-3/h1H2
InChI 密鑰
NZZFYRREKKOMAT-UHFFFAOYSA-N
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訊號詞
Warning
危險聲明
危險分類
Acute Tox. 4 Oral - Aquatic Chronic 3
儲存類別代碼
10 - Combustible liquids
水污染物質分類(WGK)
WGK 3
閃點(°F)
230.0 °F - closed cup
閃點(°C)
110 °C - closed cup
Journal of dentistry, 38(2), 123-130 (2009-10-14)
This study examined the surface free energy of enamel treated with the single-step self-etching adhesives Bond Force, Clearfil tri-S Bond and G-Bond. The labial enamel surfaces of bovine mandibular incisors were wet ground with #180-grit, #600-grit and #2000-grit silicon carbide
Physical chemistry chemical physics : PCCP, 13(24), 11671-11677 (2011-05-20)
Flash photolysis (FP) coupled to resonance fluorescence (RF) was used to measure the absolute rate coefficients (k(1)) for the reaction of OH(X(2)Π) radicals with diiodomethane (CH(2)I(2)) over the temperature range 295-374 K. The experiments involved time-resolved RF detection of the
The journal of physical chemistry. A, 116(11), 2713-2722 (2011-12-01)
We investigate the structural dynamics of iodine elimination reaction of 1,2-diiodoethane (C(2)H(4)I(2)) in cyclohexane by applying time-resolved X-ray liquidography (TRXL). The TRXL technique combines structural sensitivity of X-ray diffraction and 100 ps time resolution of X-ray pulses from synchrotron and
Journal of combinatorial chemistry, 12(3), 327-331 (2010-03-12)
A mild and efficient protocol for the synthesis of a 2,6-disubstituted pyrimidine-5-carboxylate library via a Morita-Baylis-Hillman (MBH) adduct is described. Herein, the three step methodology involves the use of substituted alpha-iodomethylene beta-keto ester intermediates obtained after oxidation of the MBH
Journal of the American Chemical Society, 127(36), 12440-12441 (2005-09-08)
A new family of zinc carbenoids derived from phosphoric acids was developed and used in the cyclopropanation of allylic alcohols and ethers and also of unfunctionalized olefins. The use of the chiral phosphoric acid of a 3,3'-disubstituted BINOL leads to
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