ライフサイエンスコーパス: methylene chloride

1 silyl enol ethers are surprisingly stable in methylene chloride.

2 uefortine C were extracted from samples with methylene chloride.

3 l carbamate, and the occupational carcinogen methylene chloride.

4 ronoabsorptometry of Cl2FeS2MoS2FeCl2(2-) in methylene chloride.

5 ond complex between U(H)(+) and HU(H)H(+) in methylene chloride.

6 d 36 cm-1, respectively, relative to that in methylene chloride.

7 with CXF spectra in aqueous solution and in methylene chloride.

8 Methylene chloride or products containing methylene chloride.

9 the course of an unconventional synthesis in methylene chloride.

10 However, concerns have emerged over methylene chloride, a chemical used in decaffeination, d

11 a 5-congener mixture in relatively volatile methylene chloride, a methylene chloride extract of free

12 kyne, Et(2)Zn, and (S)-1,1'-bi-2-naphthol in methylene chloride allows the generation of an alkynylzi

13 e ket as the freezing points of the solvents methylene chloride and acetonitrile were approached.

14 a functional group, has been investigated in methylene chloride and acetonitrile.

15 k copolymers were assembled by dissolving in methylene chloride and allowing the solvent to evaporate

16 at is an undesirable solvent with the use of methylene chloride and N,N-dimethylformamide being parti

17 Among these, methylene chloride and N-methyl-2-pyrrolidone were most

18 ulfonic (triflic) acid compared with aprotic methylene chloride and sulfolane solutions.

19 uintile of diesel, lead, manganese, mercury, methylene chloride, and an overall measure of metals wer

20 ibrium measurements in trifluoroacetic acid, methylene chloride, and ethyl acetate demonstrated that

21 as explored in three solvents: acetonitrile, methylene chloride, and methanol.

22 chloridate and excess nucleoside in pyridine/methylene chloride at 0 degree C to give 3 in 82% yield.

23 e (for 2) with phosphorus oxychloride in dry methylene chloride at 0 degree C with the addition of tr

24 The particulate matter was extracted using methylene chloride, back extracted into aqueous solution

25 to methylene chloride or products containing methylene chloride between 1980 and 2018.

26 We also obtained data about nonfatal methylene chloride cases from the American Association o

27 n Control Centers documented 37 201 nonfatal methylene chloride cases, with a decrease in the annual

28 c solvents studied were acetonitrile (MeCN), methylene chloride, chloroform, and tetrahydrofuran (THF

29 mixture of hexafluoro-2-propanol (HFIP) and methylene chloride (DCM) is described.

30 A 75/25 acid capped (13 kDa Mw) dissolved in methylene chloride (DCM) was spray-dried before washing

31 to 8-fluoro-2'-deoxyadenosine using TASF in methylene chloride demonstrates the compatibility of des

32 e common organic solvents evaluated (hexane, methylene chloride, diethylether, chloroform, methylisob

33 ence anions in seven solvents: acetonitrile, methylene chloride, dimethylformamide, tetrahydrofuran,

34 Methylene chloride/ethyl acetate/formic acid (6:10:1, v/

35 Prevention of fatalities associated with methylene chloride exposure should emphasize the use of

36 in relatively volatile methylene chloride, a methylene chloride extract of freeze-dried mussel (Mytil

37 2, 3-dimethyl-2-butene in the gas phase and methylene chloride extracts of 2,3-dimethyl-2-butanol an

38 xt-4 and roots: Ext-5), in addition to their methylene chloride fractions of roots extracts (F-6 and

39 ed significant cytotoxicity, among them, the methylene chloride fractions of roots of J. variegata (F

40 igh quantum yields (60-99%) were observed in methylene chloride in addition to large Stokes shifts (9

41 was increased to 0.08-0.24 with 1000 ppm of methylene chloride in the drift gas.

42 Likewise, nine of 24 methylene chloride-induced hepatocellular neoplasms and

43 Methylene chloride is a halogenated organic solvent wide

44 However, the oxidation of U(H)H in methylene chloride is reversible at higher concentration

45 effects of carbon monoxide (CO) induction by methylene chloride (MC).

46 the US that were associated with exposure to methylene chloride or products containing methylene chlo

47 Methylene chloride or products containing methylene chlo

48 be selectively prepared simply by selecting methylene chloride or THF as the reaction solvent, respe

49 rs were the most common products involved in methylene chloride-related fatalities (n = 60).

50 e label warnings and occupational standards, methylene chloride-related fatalities continue to occur

51 From 1980 to 2018, 85 methylene chloride-related fatalities were identified in

52 To determine characteristics of the methylene chloride-related fatalities, we recorded demog

53 The potential cancer risk from methylene chloride residue in decaffeinated coffee remai

54 rs associated with NNK, vinyl carbamate, and methylene chloride, respectively.

55 zation is more favorable, whereas GaCl(3) in methylene chloride shifts the chemoselectivity toward a

56 Sequestration of a methylene chloride solution of the Ds-pip complex from a

57 ions persist for days at room temperature in methylene chloride solution.

58 s observed in toluene, C(6)D(6), heptane, or methylene chloride solutions.

59 PVF = poly(vinylferrocene)) films exposed to methylene chloride solutions.

60 plementary oligoamides in not only nonpolar (methylene chloride) solutions but also highly competitiv

61 the photolysis reactions were carried out in methylene chloride, solvent binding competitive with hyd

62 regulations to address the toxic effects of methylene chloride use for consumers and workers, there

63 velengths could be affected by swelling with methylene chloride vapor.

64 mines in N,N-dimethylformamide, methanol, or methylene chloride/water (phase-transfer conditions) yie

65 acid (DCA) and trichloroacetic acid (TCA) in methylene chloride were found to be 3% DCA >> 15% DCA >

66 solvents as revealed by (113)Cd NMR in d(2)-methylene chloride, which displays (111)Cd-(113)Cd coupl

67 solutions of nonhydrated glyoxals (16k-m) in methylene chloride with Deoxofluor produced the tetraflu