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Detail of "1467-79-4"

  • CAS Number:
  • 1467-79-4
  • Name:
  • Cyanamide,N,N-dimethyl-

  • Molecular Structure:
  • Formula:
  • C3H6 N2
  • Molecular Weight:
  • 70.11
  • Synonyms:
  • Cyanamide,dimethyl- (6CI,7CI,8CI,9CI); Cyanodimethylamine; Dimethylaminocarbonitrile;Dimethylcyanamide; N,N-Dimethylcyanamide; N-Cyano-N-methylmethanamine;N-Cyanodimethylamine; NSC 7765
  • Density:
  • 0.89g/cm3
  • Boiling Point:
  • 163.5°Cat760mmHg
  • Flash Point:
  • 58.3°C
  • Hazard Symbols:
  • T
  • Risk Codes:
  • R23/24/25;R36/37/38;
  • Safety:
  • Poison by ingestion, skin contact, and intraperitoneal routes. Moderately toxic by inhalation. Flammable when exposed to heat, flame, or oxidizers. Can react with oxidizing materials. To fight fire, use foam, CO2, or dry chemical. When heated to decomposition or in reaction with water or steam it produces toxic fumes of NOx and CN and flammable vapors. See also CYANIDE. Details

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CAS No.1467-79-4 Dimethylcyanamide

Assay:98%

Supplier:Hangzhou Dayangchem Co., Ltd. [ China (Mainland)]

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Address:B/2601 Fuli Building, 328# WenEr Rd. Hangzhou City 310012 China

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CAS No.1467-79-4 Cyanamide,N,N-dimethyl-

Dimethylcyanamide

Supplier:Synthon Chemicals GmbH & Co. KG [ Germany]

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Tel:+49 3494 636983

Address:Chemiepark Bitterfeld-Wolfen, Areal A, Werkstattstrasse 10

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CAS No.1467-79-4 Cyanamide,N,N-dimethyl-

Supplier:Far Chemical [ United States]

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Tel:321-723-6160

Address:Palm Bay, Florida 32905-2548

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Reference

Synthesis of 1,3-dioxin-4-ones and their use in synthesis
Synthesis of 1,3-dioxin-4-ones and their use in synthesis. XI. 2,2-Dimethyl-1,3-dioxin-4-one as a synthetic equivalent of formylketene: synthesis of heterocyclic compounds. Sato, Masayuki; Yoneda, Naoki; Kaneko, Chikara (Pharm. Inst., Tohoku Univ., Sendai 980, Japan). Chem. Pharm. Bull., 34(2), 621-7 (English) 1986. 141-90-2 which is the cas registry number is also used here. CODEN: CPBTAL. ISSN: 0009-2363. DOCUMENT TYPE: Journal CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) Cycloaddn. of formylketene, generated in situ by thermolysis of dimethyldioxinone I with Ph2C:NCH2Ph yields benzyldiphenyloxazinone II. Analogous reactions with a carbodiimide, cyanamide, and ketene acetal afford the corresponding 4+2 cycloadducts, e.g. III and IV. Reaction of formylketene with 3-amino-2-butenamides affords 4-hydroxy-2-pyridones, e.g., V (R = H, CH2Ph), having a two-C unit at the 3-position. .
Electron spin resonance studies of the effects of ionizing radiation on cyanamide and dimethylcyanamide
Electron spin resonance studies of the effects of ionizing radiation on cyanamide and dimethylcyanamide. Chandra, Harish; Mishra, Shuddhodan P.; Symons, Martyn C. R. (Dep. Chem., Univ. Leicester, Leicester LE1 7RH, UK). Chem. Phys. Lett. 420-04-2 and 1467-79-4 are cas registry numbers of chemicals which are used as reagents here., 134(4), 307-10 (English) 1987. CODEN: CHPLBC. ISSN: 0009-2614. DOCUMENT TYPE: Journal CA Section: 74 (Radiation Chemistry, Photochemistry, and Photographic and Other Reprographic Processes) A range of radicals was obtained from g-irradiated pure H2NCN and Me2NCN and from solns. The reaction mechanism favored electron capture or electron loss. Those well characterized by ESR spectroscopy included H2NHC:N, Me2NCN+ and Me2N×. .
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