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Detail of "5159-41-1"

  • CAS Number:
  • 5159-41-1
  • Name:
  • Benzenemethanol,2-iodo-

  • Superlist Name:
  • 2-Iodobenzyl alcohol
  • Molecular Structure:
  • Formula:
  • C7H7IO
  • Molecular Weight:
  • 234.03
  • Synonyms:
  • Benzylalcohol, o-iodo- (6CI,7CI,8CI);1-Hydroxymethyl-2-iodobenzene;2-(Hydroxymethyl)-1-iodobenzene;2-(Hydroxymethyl)iodobenzene;2-Iodobenzenemethanol;2-Iodophenylmethanol;o-Iodobenzyl alcohol;
  • EINECS:
  • 225-933-2
  • Density:
  • 1.867 g/cm3
  • Melting Point:
  • 89-92 °C(lit.)
  • Boiling Point:
  • 288.3 °C at 760 mmHg
  • Flash Point:
  • 128.2 °C
  • Appearance:
  • white to yellow or pinkish needle-like powder
  • Hazard Symbols:
  • IrritantXi
  • Risk Codes:
  • 36/38
  • Safety:
  • 22-24/25 Details

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CAS No.5159-41-1 2-Iodobenzyl alcoholCompetitive Product

2-Iodobenzyl alcohol

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

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CAS No.5159-41-1 2-Iodobenzyl alcohol

(2-iodophenyl)methanol

Supplier:Weihao Chemtech (ChangZhou) Co., Ltd. [ China (Mainland)]

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CAS No.5159-41-1 2-Iodobenzyl alcohol

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CAS No.5159-41-1 2-Iodobenzyl alcohol

2-Iodobenzyl alcohol

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CAS No.5159-41-1 2-Iodobenzyl alcohol

MF:IC6H4CH2OH MW:234.03 Assay: ≥99.0% MP: 89-92 °C

Supplier:Nanjing Carbonde Tech Co., Ltd. [ China (Mainland)]

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CAS No.5159-41-1 2-Iodobenzyl alcohol

Supplier:Qingdao WANSHENGDA Chemical Co,ltd [ China (Mainland)]

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Supplier:Qingdao Hongfu Import & Export Co., Ltd. [ China (Mainland)]

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CAS No.5159-41-1 2-Iodobenzyl alcohol

Supplier:Dalian Shenghongjie Chemicals co,.ltd [ China (Mainland)]

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CAS No.5159-41-1 2-Iodobenzyl alcohol

Supplier:Aemon Chemical Technology Co. Limited [ China (Mainland)]

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Reference

Highly Regioselective Radical Cyclizations of Allenamides
Highly Regioselective Radical Cyclizations of Allenamides. Shen, Lichun; Hsung, Richard P. (Department of Chemistry, University of Minnesota, Minneapolis, MN 55455, USA). Organic Letters, 7(5), 775-778 (English) 2005 American Chemical Society. CODEN: ORLEF7. ISSN: 1523-7060. DOCUMENT TYPE: Journal CA Section: 27 (Heterocyclic Compounds (One Hetero Atom)) The first radical intramol. cyclizations of allenamides, e.g. I (R = Me, MeO, Me3CO, Me2N, H2C:CHCH2CH2, etc.), are described. These reactions are highly regioselective for the central carbon of the allenic moiety, leading to an efficient prepn. of nitrogen heterocycles such as isoquinolines, and carbocycles such as indene and naphthalene derivs. The exo-cyclization mode could also be achieved in some cases, leading to the synthesis of isoindoles.In this experiment, several chemicals are used like 5159-41-1 The feasibility of a tandem radical cyclization using allenamide is also established. .
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