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Detail of "13429-83-9"

  • CAS Number:
  • 13429-83-9
  • Name:

  • (1S)-(-)-Camphanic acid

  • Molecular Structure:
  • Formula:
  • C10H14O4
  • Molecular Weight:
  • 198.22
  • Synonyms:
  • 2-Oxabicyclo[2.2.1]heptane-1-carboxylicacid, 4,7,7-trimethyl-3-oxo-, (1S)- (8CI);(-)-Camphanic acid;(-)-w-Camphanic acid;2-Oxabicyclo[2.2.1]heptane-1-carboxylicacid, 4,7,7-trimethyl-3-oxo-, (1S,4R)-;(1S)-Camphanic acid;(1S,4R)-(-)-Camphanic acid;(1S,4R)-w-Camphanic acid;(S)-Camphanic acid;Camphanic acid;w-Camphanic acid, (-)-;
  • EINECS:
  • 236-552-6
  • Density:
  • 1.296 g/cm3
  • Melting Point:
  • 201-205 °C
  • Appearance:
  • white to slightly beige crystalline powder
  • Hazard Symbols:
  • IrritantXi,HarmfulXn
  • Risk Codes:
  • 36/37/38-20/21/22
  • Safety:
  • 22-24/25-37/39-26-36 Details
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CAS No.13429-83-9 (1S)-(-)-Camphanic acidCompetitive Product

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CAS No.13429-83-9 (1S)-(-)-Camphanic acid

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CAS No.13429-83-9 (1S)-(-)-Camphanic acid

Chemical Name: (-)-CAMPHANIC ACID CAS No. 13429-83-9 Molecular Formula: C10H14O4 Formula Weight: 198.22 Property mp : 201-205 °C Safety Hazard Codes : Xi Risk Statements : 36/37/38 Safety Statements : 22-24/25 WGK Germany : 3

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CAS No.13429-83-9 (1S)-(-)-Camphanic acid

Product name:(1S)-(-)-Camphanic acid cas# :13429-83-9 Assay:98% min Appearance:white powder E-mail: John_peng@infine-chem.com

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CAS No.13429-83-9 (1S)-(-)-Camphanic acid

(1s)-(-)-camphanic acid

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(1S)-(-)-CAMPHANIC ACID

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CAS No.13429-83-9 (1S)-(-)-Camphanic acid

C10H14O4 99%

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(1S)-(-)-Camphanic acid

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(-)-CAMPHANIC ACID

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(-)-CAMPHANIC ACID

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(-)-CAMPHANIC ACID

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Reference

Stereochemistry of the metabolism of the DNA base thymine and the drug 5-fluorouracil
Stereochemistry of the metabolism of the DNA base thymine and the drug 5-fluorouracil. Gani, David; Hitchcock, Peter B.; Young, Douglas W. (Sch. Chem. Mol. Sci., Univ. Sussex, Brighton BN1 9QJ, UK). J. Chem. Soc., Chem.Several substances with their cas registry numbers 88099-60-9 and 13429-83-9 may be metioned in this study. Commun., (16), 898-900 (English) 1983. CODEN: JCCCAT. ISSN: 0022-4936. DOCUMENT TYPE: Journal CA Section: 7 (Enzymes) Section cross-reference(s): 75 Both thymine (I; R = Me) and the anticancer drug, 5-fluorouracil (I; R = F) (II), were reduced by dihydrothymine dehydrogenase by overall trans addn. of H, at the si-face at C-5 and the si-face at C-6. The structure of the amide (III) of the redn. product of II was detd. by x-ray crystallog. .
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