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Detail of "53242-88-9"

  • CAS Number:
  • 53242-88-9
  • Name:
  • 4-(4-Chloro-benzyl)-2H-phthalazin-1-one

  • Molecular Structure:
  • Formula:
  • C15H11ClN2O
  • Molecular Weight:
  • 270.72
  • Synonyms:
  • 1(2H)-Phthalazinone,4-p-chlorobenzyl- (6CI);4-(4-Chlorobenzyl)-1(2H)-phthalazinone;4-[(4-Chlorophenyl)methyl]-1(2H)-phthalazinone;1(2H)-Phthalazinone,4-[(4-chlorophenyl)methyl]-;4-(4-Chlorobenzyl)-1,2-dihydrophthalazine-1-one;
  • EINECS:
  • 258-445-3
  • Density:
  • 1.32 g/cm3
  • Boiling Point:
  • 522.3 °C at 760 mmHg
  • Flash Point:
  • 269.7 °C

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CAS No.53242-88-9 4-(4-Chloro-benzyl)-2H-phthalazin-1-oneCompetitive Product

Molecular Formula: C15H11Cl N2 O Molecular Weight: 270.72 EINECS: 258-445-3 Density: 1.32 g/cm3 Boiling Point: 522.3 oC at 760 mmHg Flash Point: 269.7 oC

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CAS No.53242-88-9 4-(4-Chloro-benzyl)-2H-phthalazin-1-one

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CAS No.53242-88-9 4-(4-Chloro-benzyl)-2H-phthalazin-1-one

TOXICITY: N/A SAFETY: N/A Production: N/A Others: APIChem is a professional supplier of Research Chemicals. We have this item in stock, purity: 98%.

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CAS No.53242-88-9 4-(4-Chloro-benzyl)-2H-phthalazin-1-one

4-(4-Chloro-benzyl)-2H-phthalazin-1-one

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4-(4-Chloro-benzyl)-2H-phthalazin-1-one

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CAS No.53242-88-9 4-(4-Chloro-benzyl)-2H-phthalazin-1-one

4-(4-Chloro-benzyl)-2H-phthalazin-2-one

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Reference

Reactions of hydrazine hydrate and phenylhydrazine with thiophthalic anhydride, substituted phthalides and 2-dithiobenzoyl
Reactions of hydrazine hydrate and phenylhydrazine with thiophthalic anhydride, substituted phthalides and 2-dithiobenzoyl. Omran, S. M. A. E.; Salem, M. R. M.; Harb, Nagwa S. (Fac. Sci., Ain Shams Univ., Cairo, Egypt). Egypt. J. Chem., Volume Date 1974, 17(6), 731-9 (English) 1976. CODEN: EGJCA3. 57835-95-7 and 53242-88-9 which are cas registry numbers of chemicals are mentioned. DOCUMENT TYPE: Journal CA Section: 22 (Physical Organic Chemistry) H2NNH2.H2O and PhNHNH2 react with thiophthalic anhydride to give phthalaz-1,4-dione (I) and N-anilinophthalimide, resp. H2NNH2.H2O reacts with phthalides II (R = H, Cl, OMe; X = O, S) to give III (same R); PhNHNH2 reacts with II (R = H, Cl; X = O, S) to give IV (same R). H2NNH2.H2O reacts with V to give a mixt. of VI (X = O, S; R = H); PhNHNH2 reacts with V to give VI (X = O; R = Ph). .
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