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Detail of "6214-65-9"

  • CAS Number:
  • 6214-65-9
  • Name:

  • 2,4(1H,3H)-Pyrimidinedione,5-acetyl-

  • Superlist Name:
  • 5-Acetyluracil
  • Molecular Structure:
  • Formula:
  • C6H6 N2 O3
  • Molecular Weight:
  • 154.12
  • Synonyms:
  • Uracil,5-acetyl- (6CI,7CI,8CI); 5-Acetouracil; 5-Acetyluracil; NSC 34716
  • Melting Point:
  • 278 °C (dec.)(lit.)
  • Boiling Point:
  • 265°C
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CAS No.6214-65-9 5-Acetyluracil

Supplier:Changzhou Ansciep Chemical Co.,Ltd. [ China (Mainland)]

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CAS No.6214-65-9 5-Acetyluracil

Assay:98%  Appearance:liquid or so...  Package:On requireme...

Supplier:AOPHARM [ China (Mainland)]

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CAS No.6214-65-9 5-Acetyluracil

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

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CAS No.6214-65-9 5-Acetyluracil

Supplier:Shenyang Meiyao Chemical Co., Ltd., [ China (Mainland)]

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CAS No.6214-65-9 5-Acetyluracil

Supplier:Changzhou Sohon Chemtech Co., Ltd. [ China (Mainland)]

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CAS No.6214-65-9 5-Acetyluracil

5-Acetyluracil

Supplier:Jiangsu hengjiu Pharmtech Co., Ltd. [ China (Mainland)]

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CAS No.6214-65-9 5-acetyluracil

5-acetyluracil

Supplier:lianyungang scipharm technology co.,ltd [ China (Mainland)]

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CAS No.6214-65-9 5-Acetyluracil

Supplier:Tianjin Chemlike Scientific Co., Ltd. [ China (Mainland)]

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CAS No.6214-65-9 5-Acetyluracil

Supplier:SYHAI CHEMICAL [ China (Mainland)]

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Reference

Incorporation of 5-substituted uracil derivatives into nucleic acids
Incorporation of 5-substituted uracil derivatives into nucleic acids. III. Synthesis of 5-substituted uracils derived from 5-acetyluracil. Bleackley, R. C.; Jones, A. S.; Walker, R. T. (Dep. Chem., Univ.There are some reagents with their cas registry numbers 62785-92-6 and 6214-65-9 are used in this study. Birmingham, Birmingham, Engl.). Tetrahedron, 32(22), 2795-7 (English) 1976. CODEN: TETRAB. DOCUMENT TYPE: Journal CA Section: 28 (Heterocyclic Compounds (More Than One Hetero Atom)) Bromination of 5-acetyluracil gave 73% 5-(bromoacetyl)uracil (I) which on redn. with NaBH4 gave 5-(2-hydroxyethyl)uracil. I showed low antibacterial activity against Staphylococcus aureus, Streptococcus faecalis, and Escherichia coli in nutrient broth, and appreciable activity (.apprx.6 .mu.g/mL) against E. coli in a medium contg. inorg. salts, glucose, and thymine. I was not incorporated into the DNA of E. coli. Bromination of 5-vinyluracil gave 85% E-5-(2-bromovinyl)uracil (II) which with KOCMe3 gave 58% furanopyrimidinone II and on redn. with Na in liq. NH3 gave 5-ethyluracil. .
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