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Chemical Structure| 108-30-5 Chemical Structure| 108-30-5
Chemical Structure| 108-30-5

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Succinic anhydride is a cyclic anhydride and a nonclaevable ADC linker extracted from patent WO2009064913A1. Succinic anhydride can react with compound 4 of the patent to link the prodrug to an amine or hydroxy 1 group of a targeting polypeptide.

Synonyms: Succinyl Oxide; SA

4.5 *For Research Use Only !

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Product Details of Succinic anhydride

CAS No. :108-30-5
Formula : C4H4O3
M.W : 100.07
SMILES Code : O=C(CC1)OC1=O
Synonyms :
Succinyl Oxide; SA
MDL No. :MFCD00005525
InChI Key :RINCXYDBBGOEEQ-UHFFFAOYSA-N
Pubchem ID :7922

Safety of Succinic anhydride

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H302-H314-H317-H334
Precautionary Statements:P501-P272-P260-P270-P264-P280-P284-P342+P311-P362+P364-P303+P361+P353-P333+P313-P301+P330+P331-P301+P312+P330-P304+P340+P310-P305+P351+P338+P310-P405
Class:8
UN#:3261
Packing Group:

Application In Synthesis of Succinic anhydride

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Upstream synthesis route of [ 108-30-5 ]
  • Downstream synthetic route of [ 108-30-5 ]

[ 108-30-5 ] Synthesis Path-Upstream   1~8

  • 1
  • [ 1003-09-4 ]
  • [ 108-30-5 ]
  • [ 52240-28-5 ]
References: [1] Journal of Organic Chemistry, 2001, vol. 66, # 22, p. 7283 - 7286.
[2] Organic Syntheses, 2002, vol. 79, p. 204 - 204.
[3] Journal of the Chemical Society, 1954, p. 4162,4165.
[4] Recueil des Travaux Chimiques des Pays-Bas, 1950, vol. 69, p. 1083,1103.
[5] Nippon Kagaku Zasshi, 1957, vol. 78, p. 779,783[6] Chem.Abstr., 1960, p. 22559.
  • 2
  • [ 1003-09-4 ]
  • [ 108-30-5 ]
  • [ 80885-88-7 ]
  • [ 52240-28-5 ]
References: [1] Patent: US4299769, 1981, A, .
  • 3
  • [ 108-30-5 ]
  • [ 1165952-91-9 ]
  • [ 6708-37-8 ]
References: [1] Australian Journal of Chemistry, 1981, vol. 34, # 8, p. 1719 - 1727.
  • 4
  • [ 108-30-5 ]
  • [ 57-14-7 ]
  • [ 1596-84-5 ]
References: [1] Journal of Organic Chemistry, 1973, vol. 38, p. 2058 - 2061.
  • 5
  • [ 108-30-5 ]
  • [ 2216-69-5 ]
  • [ 3562-99-0 ]
YieldReaction ConditionsOperation in experiment
86.4% With aluminum (III) chloride In dichloromethane at 33 - 37℃; for 6 h; 15.8 g of 1-methoxynaphthalene and 10.0 g of succinic anhydride were dissolved in 120 mL of dichloromethane,Stir,Cooling to 1 ~ 3 ° C,Divided into three batches of anhydrous aluminum trichloride 15.0 grams,The addition process takes about 20 minutes,The solution was then heated to 35 ± 2 ° C,Insulation reaction 6 hours (5.5 ~ 6.5 hours range),After the reaction is complete,The reaction solution was poured into an ice-water mixture (200 g of ice and 300 g of water) for 30 minutes,Standing, analysiscrystal,Filter,The filtrate was heated and distilled to recover dichloromethane,The cake is the crude of the ketone ketone;And then the crude ketoprofen water as a solvent by 2-3 times recrystallization,Activated carbon decolorization,Demon ketone boutique.The mass of the present product of the chamballone was 22.3 g,Melting point of 176 ~ 179 ° C,The yield was 86.4percent.
References: [1] Patent: CN104370734, 2016, B, . Location in patent: Paragraph 0016-0018.
[2] Helvetica Chimica Acta, 1932, vol. 15, p. 907,914.
[3] Journal of the University of Bombay, Science: Physical Sciences, Mathematics, Biological Sciences and Medicine, 1936, vol. 5/2, p. 73,75.
[4] Journal of the American Chemical Society, 1940, vol. 62, p. 2750,2752.
[5] Journal of the American Chemical Society, 1951, vol. 73, p. 897,899.
[6] Journal of the American Chemical Society, 1951, vol. 73, p. 326,327.
[7] Kogyo Kagaku Zasshi, 1953, vol. 56, p. 887,889[8] Chem.Abstr., 1955, p. 6904.
[9] Journal of the American Chemical Society, 1936, vol. 58, p. 2314,2316.
[10] Bulletin de la Societe Chimique de France, 1968, p. 627 - 631.
[11] Fortschr. Teerfarbenfabr. Verw. Industriezweige, vol. 14, p. 285.
  • 6
  • [ 108-30-5 ]
  • [ 75-15-0 ]
  • [ 7446-70-0 ]
  • [ 2216-69-5 ]
  • [ 3562-99-0 ]
References: [1] Journal of the American Chemical Society, 1936, vol. 58, p. 2314,2316.
[2] Helvetica Chimica Acta, 1932, vol. 15, p. 907,914.
[3] Journal of the University of Bombay, Science: Physical Sciences, Mathematics, Biological Sciences and Medicine, 1936, vol. 5/2, p. 73,75.
  • 7
  • [ 108-30-5 ]
  • [ 7446-70-0 ]
  • [ 630-20-6 ]
  • [ 2216-69-5 ]
  • [ 3562-99-0 ]
References: [1] Journal of the American Chemical Society, 1936, vol. 58, p. 2314,2316.
[2] Helvetica Chimica Acta, 1932, vol. 15, p. 907,914.
[3] Journal of the University of Bombay, Science: Physical Sciences, Mathematics, Biological Sciences and Medicine, 1936, vol. 5/2, p. 73,75.
  • 8
  • [ 108-30-5 ]
  • [ 7446-70-0 ]
  • [ 98-95-3 ]
  • [ 2216-69-5 ]
  • [ 3562-99-0 ]
References: [1] Journal of the American Chemical Society, 1936, vol. 58, p. 2314,2316.
[2] Helvetica Chimica Acta, 1932, vol. 15, p. 907,914.
[3] Journal of the University of Bombay, Science: Physical Sciences, Mathematics, Biological Sciences and Medicine, 1936, vol. 5/2, p. 73,75.
 

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