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Detail of "5900-55-0"

  • MSDS Download
  • CAS Number:
  • 5900-55-0
  • Name:
  • Acetamide,N-(5-chloro-2-methylphenyl)-

  • Superlist Name:
  • N-(5-Chloro-2-methylphenyl)acetamide
  • Molecular Structure:
  • Formula:
  • C9H10ClNO
  • Molecular Weight:
  • 183.63
  • Synonyms:
  • o-Acetotoluidide,5'-chloro- (6CI,7CI,8CI);2-Acetamido-4-chlorotoluene;5-Chloro-o-acetotoluidide;5'-Chloro-2'-methylacetanilide;N-(5-Chloro-2-methylphenyl)acetamide;NSC 404301;
  • Density:
  • 1.218 g/cm3
  • Boiling Point:
  • 319.6 °C at 760 mmHg
  • Flash Point:
  • 147.1 °C

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CAS No.5900-55-0 N-(5-Chloro-2-methylphenyl)acetamide

Assay:98%

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

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CAS No.5900-55-0 N-(5-Chloro-2-methylphenyl)acetamide

4.9 gram in stock of Specs ID AC-907/25004932.

Supplier:SPECS [ Netherlands]

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Reference

Synthesis of dyes from 2-chloro-5-methyl-1,4-phenylenediamine
Synthesis of dyes from 2-chloro-5-methyl-1,4-phenylenediamine. Sebe, Ion; Popescu, Ioan Dan; Ganea, Adriana; Calota, Ioana (Inst. Politeh., Bucharest, Rom.). Ind. Usoara: Text., Tricotaje, Confectii Text., 35(8), 368-71 (Romanian) 1984. CODEN: IUSAAE. DOCUMENT TYPE: Journal CA Section: 41 (Dyes, Organic Pigments, Fluorescent Brighteners, and Photographic Sensitizers) Section cross-reference(s): 40 Reaction of the title compd. (I) [5307-03-9] with bromaminic acid Na salt [6258-06-6] gave II(R1 = SO3Na, R2 = NH2)(III) [96384-10-0], and redn. of III with glucose gave II(R1 = H, R2 = NH2)(IV) [96384-11-1], which was chloroacetylated to form II(R1 = H, R2 = NHCOCH2Cl)(V) [96384-12-2] and then quaternized with C5H5N and ZnCl2 to give II(R1 = H, R2 = NHCOCH2NC5H5.ZnCl3)(VI) [96384-14-4]. III colored wool dark blue; IV colored polyester fibers light blue-violet; V colored polyester fibers violet; and VI colored acrylic fibers violet. All the dyeings exhibited excellent light resistance and good resistance to rubbing and heat. I was prepd. by a series of reactions involving nitrating p-toluidine (VII) [106-49-0], diazotizing nitrated VII, conducting a Sandmeyer reaction on the resulting diazonium salt to give 4-chloro-2-nitrotoluene (VIII) [89-59-8], reducing VIII to 2-amino-4-chlorotoluene (IX) [95-79-4], acetylating IX to 5-chloro-2-methylacetanilide (X) [5900-55-0], nitrating X to 2-acetylamino-4-chloro-5-nitrotoluene [13852-50-1] (plus the 3-nitro isomer), hydrolyzing the isomer mixt., sepg. 2-amino-4-chloro-5-nitrotoluene (XI) [13852-51-2], and reducing XI.
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