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Detail of "4637-24-5"

  • CAS Number:
  • 4637-24-5
  • Name:
  • N,N-Dimethylformamide dimethyl acetal

  • Molecular Structure:
  • Formula:
  • C5H13NO2
  • Molecular Weight:
  • 119.16
  • Synonyms:
  • Trimethylamine,1,1-dimethoxy- (6CI,7CI,8CI);(Dimethoxymethyl)dimethylamine;(Dimethylamino)dimethoxymethane;(Dimethylamino)formaldehyde dimethyl acetal;1,1-Dimethoxy-N,N-dimethylmethanamine;1,1-Dimethoxy-N,N-dimethylmethane amine;1,1-Dimethoxytrimethylamine;DMF dimethyl acetal;DMFDMA;Dimethoxy(dimethylamino)methane;Dimethoxy-N,N-dimethylmethanamine;Dimethyl dimethylformamide acetal;Methyl-8;N,N-Dimethyl-1,1-bis(methyloxy)methanamine;N,N-Dimethylformamide dimethylacetal;N-(Dimethoxymethyl)-N,N-dimethylamine;N-(Dimethoxymethyl)dimethylamine;a,a-Dimethoxytrimethylamine;N,N-dimethylformamide dimethyl acetal (DMF-DMA);
  • EINECS:
  • 225-063-3
  • Density:
  • 0.906 g/cm3
  • Melting Point:
  • -85 °C
  • Boiling Point:
  • 104.3 °C at 760 mmHg
  • Flash Point:
  • 7.2 °C
  • Solubility:
  • hydrolysis with water
  • Appearance:
  • clear colourless liquid
  • Hazard Symbols:
  • FlammableF, HarmfulXn, IrritantXi
  • Risk Codes:
  • 11-22-36/37/38-36/38-20-20/21/22-10
  • Safety:
  • 16-26-36/37-36/37/39-33-29-7/9 Details
  • Transport Information:
  • UN 3271 3/PG 2

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CAS No.4637-24-5 N,N-Dimethylformamide dimethyl acetalCompetitive Product

Assay:≥98%

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CAS No.4637-24-5 N,N-Dimethylformamide dimethyl acetal

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CAS No.4637-24-5 N,N-Dimethylformamide dimethyl acetal

Assay:99.5%  Appearance:powder  Package:25kg/Cardboa...Storage:1-10MT

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CAS No.4637-24-5 N,N-Dimethylformamide dimethyl acetal

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CAS No.4637-24-5 N,N-Dimethylformamide dimethyl acetal

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CAS No.4637-24-5 N,N-Dimethylformamide dimethyl acetal

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CAS No.4637-24-5 N,N-Dimethylformamide dimethyl acetal

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CAS No.4637-24-5 N,N-Dimethylformamide dimethyl acetal

N,N-Dimethylformamide dimethyl acetal

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CAS No.4637-24-5 N,N-Dimethylformamide dimethyl acetal

N,N-Dimethylformamide dimethyl acetal

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CAS No.4637-24-5 N,N-Dimethylformamide dimethyl acetal

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CAS No.4637-24-5 N,N-Dimethylformamide dimethyl acetal

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CAS No.4637-24-5 N,N-Dimethylformamide dimethyl acetal

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CAS No.4637-24-5 N,N-Dimethylformamide dimethyl acetal

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CAS No.4637-24-5 N,N-Dimethylformamide dimethyl acetal

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CAS No.4637-24-5 N,N-Dimethylformamide dimethyl acetal

Assay:99  Appearance:White crysta...

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CAS No.4637-24-5 N,N-Dimethylformamide dimethyl acetal

dimethylformamide dimethylacetal dimethylformamide dimethylacetal CAS NO.4637-24-5 Purity: 98.5% Output: 10 Tons Abbreviations: DMF-DMA; DMFA IUPAC Name:dimethoxy-N,N-dimethylmethanamine Appearance: colorless clear liquid Chemical purity: 98.5% (GC) Moisture

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CAS No.4637-24-5 N,N-Dimethylformamide dimethyl acetal

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2,5-Dibromo-3-Chloropyridine

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CAS No.4637-24-5 N,N-Dimethylformamide dimethyl acetal

N,N-Dimethylformamide dimethyl ?acetal?? (DMF-DMA)

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N,N DIMETHYL FROMAMIDE DIMETHYL ACETAL

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N-N Dimethyl Formamide Dimethyl Acetal(DMF DMA)

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N,N-DIMETHYLFORMAMIDE DIMETHYL ACETAL

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Reference

Antiherpes dimethylaminomethylenated guanine derivatives
Antiherpes dimethylaminomethylenated guanine derivatives. Ogilvie, Kelvin K. (ENS Biologicals, Inc., Can.). U.S. US 4461757 A 24 Jul 1984, 5 pp. (English). (United States of America). CODEN: USXXAM. CLASS: IC: A61K031-52; C07D473-18. NCL: 424085000. APPLICATION: US 83-468877 23 Feb 1983. DOCUMENT TYPE: Patent CA Section: 63 (Pharmaceuticals) Section cross-reference(s): 1, 28 I (R and R1 = C1-4 alkyl) or their salts, either alone or in admixt. with interferon, are used to treat herpes simplex type 1 viral infections. II [82410-32-0] was treated with Me2NCH(OMe)2 [4637-24-5] to give I(R = R1 = Me) (III) [92519-15-8]. In in vitro tests, the ED50 for III with respect to HSV-I Patton strain was 2.7 plaque forming units against concn. of drug. A 10-fold redn. in ED50 was obtained using interferon synergistic combinations with III. Topical, parenteral, eye drop, nose drop, and inhalation aerosol formulations are discussed.
Polymethine dyes with hydrocarbon bridges
Polymethine dyes with hydrocarbon bridges. Enamine ketones in the chemistry of cyanine dyes. Slominskii, Yu. L.; Radchenko, I. D.; Popov, S. V.; Tolmachev, A. I. (Inst. Org. Khim., Kiev, USSR). Zh. Org. Khim., 19(10), 2134-42 (Russian) 1983. CODEN: ZORKAE. ISSN: 0514-7492. DOCUMENT TYPE: Journal CA Section: 41 (Dyes, Organic Pigments, Fluorescent Brighteners, and Photographic Sensitizers) Section cross-reference(s): 24 Cyclopentanone [120-92-3] and cyclohexanone [108-94-1] react with Me2NCH(OMe)2 [4637-24-5] to give the mono- and bis(enamine) ketones, which are useful in the synthesis of merocyanines and cyanines with bridging groups. For example, 2-(dimethylaminomethylene)cyclohexanone [6135-19-9] reacted with 3-ethyl-2-methylbenzothiazolium p-toluenesulfonate [14933-76-7] in boiling pyridine to give I [88340-49-2] in 87% yield and with 2-(dimethylaminovinyl)-3-ethylbenzothiazolium iodide [17579-01-0] in pyridine contg. NaOMe to give II [88340-50-5] in 71% yield. O-Methylation of II, reaction with PhNH2, and condensation with N-ethylrhodanine [7648-01-3] gave III [88340-51-6] in 26% yield, based on II. 88340-50-5 and 3119-93-5 are just another two chemicals used in this study. 1H NMR studies showed that I and II, as well as their cyclopentanone analogs, have a pseudo-trans configuration. .
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