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Detail of "20781-23-1"

  • CAS Number:
  • 20781-23-1
  • Name:
  • Benzenemethanamine,N-[(2,4-dimethoxyphenyl)methyl]-2,4-dimethoxy-

  • Superlist Name:
  • Bis(2,4-dimethoxybenzyl)amine
  • Molecular Structure:
  • Formula:
  • C18H23NO4
  • Molecular Weight:
  • 317.38
  • Synonyms:
  • Dibenzylamine,2,2',4,4'-tetramethoxy- (8CI);Bis(2,4-dimethoxybenzyl)amine;
  • EINECS:
  • 244-037-2
  • Density:
  • 1.103 g/cm3
  • Boiling Point:
  • 443.534 °C at 760 mmHg
  • Flash Point:
  • 188.736 °C

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CAS No.20781-23-1 Bis(2,4-dimethoxybenzyl)amine

Supplier:Jinan Haohua Industry CO., LTD [ China (Mainland)]

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CAS No.20781-23-1 Bis(2,4-dimethoxybenzyl)amine

Bis(2,4-dimethoxybenyl)amine

Supplier:orichem international ltd [ China (Mainland)]

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CAS No.20781-23-1 Bis(2,4-dimethoxybenzyl)amine

Assay:98%

Supplier:Nanjing Newst Biotech Co., LTD [ China (Mainland)]

Tel:+86-25-85331029, 85306029

Address:No. 16, Dianjian Road, Nanjing, China

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CAS No.20781-23-1 Bis(2,4-dimethoxybenzyl)amine

Supplier:Haihang Industry Co.,Ltd. [ China (Mainland)]

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Address:11/F,Sangqing Fengrun BLDG,South gongye Road No.100.

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CAS No.20781-23-1 Bis(2,4-dimethoxybenzyl)amine

Supplier:shanghai sphchem co.,ltd [ China (Mainland)]

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Address:NO.133, Wuye, Yangxin Road ,Shanghai China

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CAS No.20781-23-1 Bis(2,4-dimethoxybenzyl)amine

Supplier:Fox-Chemicals GmbH [ Germany]

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Address:Bockstalstr.10A D-76327 Pfinztal-Germany

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Reference

Synthesis of a-Fluorosulfonate and a-Fluorosulfonamide Analogs of a Sulfated Carbohydrate
All Rights Reserved. Synthesis of a-Fluorosulfonate and a-Fluorosulfonamide Analogs of a Sulfated Carbohydrate. Navidpour, Latifeh; Lu, Wallach; Taylor, Scott D. (Department of Chemistry, University of Waterloo, Waterloo, ON N2L 3G1, Can.). Organic Letters, 8(24), 5617-5620 (English) 2006 American Chemical Society. 20781-23-1 and 918900-81-9 which are cas registry numbers are also used here. CODEN: ORLEF7. ISSN: 1523-7060. DOCUMENT TYPE: Journal CA Section: 33 (Carbohydrates) The first synthesis of sulfonate and sulfonamide analogs, e.g. I, of a sulfated carbohydrate in which the ester oxygen of the sulfate is replaced with a CHF or CF2 group is reported. This was accomplished by electrophilic fluorination of the protected sulfonate and sulfonamide precursors. .
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