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Detail of "1914-65-4"

  • CAS Number:
  • 1914-65-4
  • Name:

  • 1-Naphthalenecarboxylicacid, 1,2,3,4-tetrahydro-

  • Superlist Name:
  • 1,2,3,4-Tetrahydro-1-naphthoic acid
  • Molecular Structure:
  • Formula:
  • C11H12O2
  • Molecular Weight:
  • 176.21
  • Synonyms:
  • 1-Naphthoicacid, 1,2,3,4-tetrahydro- (6CI,7CI,8CI);1,2,3,4-Tetrahydro-a-naphthoic acid;1,2,3,4-Tetrahydronaphthalene-1-carboxylic acid;1-Tetralincarboxylic acid;
  • Density:
  • 1.186 g/cm3
  • Boiling Point:
  • 342.653 °C at 760 mmHg
  • Flash Point:
  • 156.408 °C
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CAS No.1914-65-4 1,2,3,4-Tetrahydro-1-naphthoic acid

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CAS No.1914-65-4 1,2,3,4-Tetrahydro-1-naphthoic acid

1,2,3,4-tetrahydro-1-naphthoic Acid, 1914-65-4

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CAS No.1914-65-4 1,2,3,4-Tetrahydro-1-naphthoic acid

1,2,3,4-Tetrahydro-1-Naphthoic Acid

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CAS No.1914-65-4 1,2,3,4-Tetrahydro-1-naphthoic acid

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CAS No.1914-65-4 1,2,3,4-Tetrahydro-1-naphthoic acid

1-Naphthalenecarboxylic acid, 1,2,3,4-tetrahydro-

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CAS No.1914-65-4 1,2,3,4-Tetrahydro-1-naphthoic acid

Product: 1,2,3,4-tetrahedro-naphthoic acid Application: Palonosetron HCl intermediate Items Specification Appearance White or pale yellow crystalline powder Specific optical rotation -59.0 - -60.0(c=1, ben) Loss on drying 1.0% max Melting point 75.0-79.0 degree C A

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CAS No.1914-65-4 1,2,3,4-Tetrahydro-1-naphthoic acid

1,2,3,4-Tetrahydro-1-naphthoic acid Size:1g;10g

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CAS No.1914-65-4 1,2,3,4-Tetrahydro-1-naphthoic acid

1,2,3,4-tetrahydro-1-naphthalenecarboxylic acid

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CAS No.1914-65-4 1,2,3,4-Tetrahydro-1-naphthoic acid

MF:C11H12O2 MW:176.21

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Reference

Separation and identification of products of tetryzolin hydrolysis
Separation and identification of products of tetryzolin hydrolysis. Nicolas, A.; Mirjolet, M.; Ziegler, J.In this study， 1914-65-4 and 84460-89-9 are also used. M. (Lab. Chim. Anal. Bromatol., Fac. Sci. Pharm. Biol., Nancy 54001, Fr.). Talanta, 31(3), 229-31 (French) 1984. CODEN: TLNTA2. ISSN: 0039-9140. DOCUMENT TYPE: Journal CA Section: 63 (Pharmaceuticals) Section cross-reference(s): 22, 64 Tetryzolin (I) [84-22-0] was subjected to acid and alk. hydrolysis and the products were isolated by TLC and identified by UV and IR spectral anal. The mass spectral fragmentation pattern of I is discussed. The alc. hydrolysis product, N-(2-aminoethyl)-1,2,3,4-tetrahydro-1-naphthamide [84460-89-9] was further hydrolyzed with acids to 1,2,3,4-tetrahydronaphthoic acid [1914-65-4] and ethylenediamine [107-15-3]. A mechanism for hydrolysis is given. .
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