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2,3-NAPHTHALENEDICARBOXYLIC ACID

  • CAS:2169-87-1
  • purity:99%
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China cas 2169-87-1 manufacturer wholesale 2,3-NAPHTHALENEDICARBOXYLIC ACID at affordable price

  • Molecular Formula: C12H8 O4
  • Molecular Weight: 216.193
  • Appearance/Colour: OFF-WHITE TO BEIGE POWDER 
  • Vapor Pressure: 2.27E-07mmHg at 25°C 
  • Melting Point: 238-240 °C (dec.)(lit.) 
  • Refractive Index: 1.7080 (estimate) 
  • Boiling Point: 407.5 °C at 760 mmHg 
  • PKA: 2.95±0.30(Predicted) 
  • Flash Point: 214.4 °C 
  • PSA: 74.60000 
  • Density: 1.454 g/cm3 
  • LogP: 2.23620 

2,3-NAPHTHALENEDICARBOXYLIC ACID(Cas 2169-87-1) Usage

Synthesis Reference(s)

Journal of the American Chemical Society, 81, p. 6458, 1959 DOI: 10.1021/ja01533a032Organic Syntheses, Coll. Vol. 5, p. 810, 1973

InChI:InChI=1/C12H8O4/c13-11(14)9-5-7-3-1-2-4-8(7)6-10(9)12(15)16/h1-6H,(H,13,14)(H,15,16)/p-2

2169-87-1 Relevant articles

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Schoenberg,Fayez

, p. 104 (1958)

-

Hydrolysis of 1,8- and 2,3-naphthalic anhydrides and the mechanism of cyclization of 1,8-naphthalic acid in aqueous solutions

Barros, Teresa C.,Yunes, Santiago,Menegon, Guilherme,Nome, Faruk,Chaimovich, Hernan,Politi, Mario J.,Dias, Luis G.,Cuccovia, Iolanda M.

, p. 2342 - 2350 (2001)

Naphthalene-1,8-dicarboxylic acid, 1,8-A...

-

Altmann,J.,Ginsburg,D.

, p. 93 - 100 (1971)

-

-

Scott

, p. 6332 (1953)

-

-

Waldmann

, p. 150 (1930)

-

New Derivatizing Agents for Amino Acids and Peptides. 1. Facile Synthesis of N-Substituted 1-Cyanobenzisoindoles and Their Spectroscopic Properties

Carlson, R. G.,Srinivasachar, K.,Givens, R. S.,Matuszewski, B. K.

, p. 3978 - 3983 (1986)

2,3-Naphthalenedicarboxaldehyde (NDA) is...

"release and catch" catalysis by tungstate species for the oxidative cleavage of olefins

Yoshimura, Yu,Ogasawara, Yoshiyuki,Suzuki, Kosuke,Yamaguchi, Kazuya,Mizuno, Noritaka

, p. 1662 - 1670 (2017/07/22)

The oxidative cleavage of olefins produc...

Preparation method of 2,3-naphthalic acid

-

, (2017/07/23)

The invention discloses a preparation me...

Formation and decomposition of N-alkylnaphthalimides: Experimental evidences and ab initio description of the reaction pathways

De Barros, Teresa Cristina,Filho, Pedro Berci,Loos, Michel,Politi, Mario Jose,Chaimovich, Hernan,Cuccovia, Iolanda Midea

experimental part, p. 385 - 397 (2011/11/06)

The kinetics of hydrolysis of 1,8-N-buty...

Rapid chemoselective deprotection of benzyl esters by nickel boride

Khurana, Jitender M.,Arora, Reema

experimental part, p. 1127 - 1130 (2009/12/03)

Benzyl esters of a variety of acids can ...

2169-87-1 Process route

anthracene
120-12-7

anthracene

formic acid
64-18-6

formic acid

naphthalene-2,3-dicarboxylic acid
2169-87-1

naphthalene-2,3-dicarboxylic acid

9,10-phenanthrenequinone
84-65-1

9,10-phenanthrenequinone

benzene-1,2-dicarboxylic acid
88-99-3,73607-73-5

benzene-1,2-dicarboxylic acid

Conditions
Conditions Yield
at 210 - 260 ℃; unter Druck;
C<sub>16</sub>H<sub>17</sub>NO<sub>3</sub>
228876-53-7

C16 H17 NO3

naphthalene-2,3-dicarboxylic acid
2169-87-1

naphthalene-2,3-dicarboxylic acid

N-Butyl-β-naphthalimide
128600-23-7

N-Butyl-β-naphthalimide

N-butylamine
109-73-9,85404-21-3

N-butylamine

Conditions
Conditions Yield
With hydrogenchloride; water; at 50 ℃; pH=4; pH-value; Time; Kinetics; aq. buffer;

2169-87-1 Upstream products

  • 108-31-6
    108-31-6

    maleic anhydride

  • 13209-15-9
    13209-15-9

    1,2-bis(dibromomethyl)benzene

  • 716-39-2
    716-39-2

    2,3-Naphthalenedicarboxylic anhydride

  • 634-36-6
    634-36-6

    1,2,3-trimethoxybenzene

2169-87-1 Downstream products

  • 716-39-2
    716-39-2

    2,3-Naphthalenedicarboxylic anhydride

  • 21815-18-9
    21815-18-9

    2-phenyl-1H-benzo[f]isoindole-1,3(2H)-dione

  • 5060-72-0
    5060-72-0

    2-(4-Chlor-phenyl)-2.3-dihydro-benz[f]indendion-(1.3)

  • 19028-96-7
    19028-96-7

    2-(3'-Methylphenyl)-2,3-dihydrobenz inden-1,3-dion

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