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Detail of "3460-49-9"

  • CAS Number:
  • 3460-49-9
  • Name:

  • Benzene,1-ethoxy-4-isothiocyanato-

  • Superlist Name:
  • 4-Ethoxyphenyl isothiocyanate
  • Molecular Structure:
  • Formula:
  • C9H9NOS
  • Molecular Weight:
  • 179.24
  • Synonyms:
  • Isothiocyanicacid, p-ethoxyphenyl ester (6CI,8CI);Phenetole, p-isothiocyanato- (6CI);1-Ethoxy-4-isothiocyanatobenzene;1-Isothiocyanato-4-ethoxybenzene;NSC 108217;p-Ethoxyphenyl isothiocyanate;
  • EINECS:
  • 222-410-0
  • Density:
  • 1.068 g/cm3
  • Melting Point:
  • 60-61 °C
  • Boiling Point:
  • 288.661 °C at 760 mmHg
  • Flash Point:
  • 128.378 °C
  • Hazard Symbols:
  • CorrosiveC,ToxicT,IrritantXi
  • Risk Codes:
  • 20/21/22-36/37/38
  • Safety:
  • 26-36/37/39 Details
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CAS No.3460-49-9 4-Ethoxyphenyl isothiocyanate

4-ethoxyphenyl isothiocyanate

Supplier:FAR Chemical's [ United Kingdom]

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CAS No.3460-49-9 4-Ethoxyphenyl isothiocyanate

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Supplier:FAR Chemical [ United States]

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Tel:321-723-6160

Address:2210 Wilhelmina Ct, NE Palm Bay, Florida 32905-2548

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CAS No.3460-49-9 4-Ethoxyphenyl isothiocyanate

Supplier:Far Chemical [ United States]

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Tel:321-723-6160

Address:Palm Bay, Florida 32905-2548

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CAS No.3460-49-9 4-Ethoxyphenyl isothiocyanate

Supplier:Shanghai Fchemicals Technology Co., Ltd [ China (Mainland)]

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Tel:021-36030322

Address:Room822, No.3, Wu Zhong Road, Shanghai, China

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Reference

Synthesis of some 3,5-diarylimino-2-phenyl-1,2,4-thiadiazolidines
Synthesis of some 3,5-diarylimino-2-phenyl-1,2,4-thiadiazolidines. Oxidative debenzylation and cyclization of 1-(N,N'-diarylamidino)-3-aryl-2-benzylisothioureas. Pandey, A. K.; Singh, R.; Verma, V. K. (Sch. Appl.In this article, certain chemicals are used. Some of their cas registry numbers are 89011-24-5 and 3460-49-9 Sci., Banaras Hindu Univ., Varanasi 221005, India). Acta Chim. Hung., 114(2), 107-11 (English) 1983. CODEN: ACHUDC. DOCUMENT TYPE: Journal CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) Guanylthioureas PhNHC(:NPh)NHCSNHR (R = tolyl, ClC6H4, alkoxyphenyl, PhCH2) were converted to thiadiazolidines I in two steps. Thus, 4-MeC6H4NHCSNHC(:NPh)NHPh was treated with PhCH2Cl, and the 4-MeC6H4N:C(SCH2Ph)NHC(:NPh)NHPh obtained was treated with Br in CHCl3 to give I (R = p-tolyl). .
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