
CAS Name: 1,2,3-Propanetriol triacetate
Additional Names: glyceryl triacetate; triacetyl glycerine
Trademarks: Enzactin (Ayerst); Fungacetin (Harvey)
Percent Composition: C 49.54%, H 6.47...
Literature References: Prepd by acetylation of glycerol: Dunbar, Bolstad, J. Org. Chem. 21, 1041 (1956); by reaction of oxygen with a liquid phase mixture of allyl acetate and acetic acid using a bromide as catalyst: Keith, US 2911437 (1959 to Sinclair Refining). As an antifungal: GB 845029 (1960 to Wisc. Alumni Res. Found.). Acute toxicity: A. Wretlind, Acta Physiol. Scand. 40, 338 (1957).
CAS Name: 1,4:3,6-Dianhydro-D-glucitol
Additional Names: 1,4:3,6-dianhydrosorbitolTrademarks: Hydronol (Stuart); Ismotic (Alcon); Isobide (Nikken)
Percent Composition: C 49.31%, H 6.90%, O 4...
Literature References: Prepd by acid dehydration of D-glucitol: Haworth, Wiggins, GB 600870 (1948). Purification: Hartmann, US 3160641 (1964 to Atlas Chemical Industries). Review of prepn, structure, properties: Wiggins, Adv. Carbohydr. Chem. 5, 191-228 (1950). Stereochemistry: Cope, Shen, J. Am. Chem. Soc. 78, 3177 (1956). Conformation studies: Hopton, Thomas, Can. J. Chem. 47, 2395 (1969). Pharmacodynamics in man: Nodine et al., Clin. Pharmacol. Ther. 14, 196 (1973).
CAS Name: [7,12-Bis(1-hydroxyethyl)-3,8,13,17-tetramethyl-21H,23H-porphine-2,18-dipropanoato(4-)-N21,N22,N23,N24]mercurate(2-) disodium
Additional Names: mercuri-hematoporphyrin disodium salt; ...
Literature References: Prepd by action of mercuric acetate upon hematoporphyrin and treating the product with sodium methoxide: JP 59 1273 (1959); GB 824705 (1959 to Daiichi), C.A. 54, 9972 (1960); Obika et al., US 3004985 (1961 to Daiichi).
CAS Name: Tetrahydroxydiborane(4)
Additional Names: hypoboric acid; sub-boric acid
Percent Composition: B 24.12%, H 4.50%, O 71.39%
Literature References: Prepd by action of steam on diboron tetrachloride: Wartik, Apple, J. Am. Chem. Soc. 77, 6400 (1955); in quantitative yield by aq hydrolysis of tetraethoxydiboron at 0°: McCloskey et al., ibid. 83, 4750 (1961).
CAS Name: (Glycinato-N,O)dihydroxyaluminum
Additional Names: dihydroxy(glycinato)aluminum; aluminum aminoacetate (basic); aluminum dihydroxyaminoacetate; aluminum glycinate; glycine, aluminum s...
Literature References: Prepd by adding a soln of aluminum isopropoxide in isopropanol to an aq soln of glycine: Krantz et al., J. Pharmacol. 82, 247 (1944).
CAS Name: Hypochlorous acid 1,1-dimethylethyl ester
Additional Names: t-butyl hypochlorite
Percent Composition: C 44.25%, H 8.36%, Cl 32.65%, O 14.74%
Literature References: Prepd by adding aq tert-butyl alcohol to a cooled aq soln of NaOH and passing chlorine into the mixture: Teeter, Bell, Org. Synth. 32, 20 (1952). By adding CO2 to neutral aq tert-butyl alcohol and NaOCl satd with NaCl: Katz, US 2694722 (1954 to Bjorksten Res. Labs.).
CAS Name: 4,4'-(3H-2,1-Benzoxathiol-3-ylidene)bis[2,6-dibromo-3-methylphenol] S,S-dioxide
Additional Names: a,a-bis(3,5-dibromo-4-hydroxy-o-tolyl)-a-hydroxytoluenesulfonic acid, g-sultone; 3,3'...
Literature References: Prepd by adding bromine to a suspension of m-cresolsulfonphthalein in glacial acetic acid: Clark, Lubs, J. Wash. Acad. Sci. 5, 610 (1915); 6, 481 (1916); J. Bacteriol. 2, 110 (1917); Cohen, Biochem. J. 16, 31 (1922); 17, 535 (1923); Cohen, Public Health Rep. 38, 814 (1923); 41, 3051 (1926); Proc. Soc. Exp. Biol. Med. 20, 124 (1922); Orndorff, Purdy, J. Am. Chem. Soc. 48, 2216 (1926).
CAS Name: 2-Bromo-1-(4-bromophenyl)ethanone
Additional Names: 2,4'-dibromoacetophenone; p,a-dibromoacetophenone
Percent Composition: C 34.57%, H 2.18%, Br 57.50%, O 5.76%
Literature References: Prepd by adding bromine to p-bromoacetophenone in glacial acetic acid at below 20°: Langley, Org. Synth. coll. vol. I, 127 (2nd ed., 1941).
CAS Name: Phosphonic acid bis(phenylmethyl) ester
Additional Names: dibenzyl hydrogen phosphite; benzyl phosphite
Percent Composition: C 64.12%, H 5.77%, O 18.30%, P 11.81%
Literature References: Prepd by adding dropwise a mixture of dimethylaniline and benzyl alc to a soln of phosphorus trichloride in benzene: Atherton et al., J. Chem. Soc. 1945, 382; US 2490573 (1949 to Hoffmann-La Roche).
Additional Names: Hexamethylenetetramine tetraiodide; methenamine tetraiodide
Percent Composition: C 11.12%, H 1.87%, I 78.36%, N 8.65%
Literature References: Prepd by adding potassium mercuric iodide to an aq soln of methenamine: US 1226394 (1917).
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