ChemicalBook--->CAS DataBase List--->23405-15-4

23405-15-4

23405-15-4 Structure

23405-15-4 Structure
IdentificationBack Directory
[Name]

BZ-OSU
[CAS]

23405-15-4
[Synonyms]

BZ-OSU
BZO-OSU
TIMTEC-BB SBB005920
SUCCINIMIDO BENZOATE
Benzoyoxysuccinimide
BENZOYLOXYSUCCINIMIDE
N-Succinimidyl Benzoate
N-(BENZOYLOXY)SUCCINIMIDE
N-ALPHA-BENZOYOXYSUCCINIMIDE
N-(Benzoyloxy)succinimide >
N-(Benzoyloxy)succinimide,97%
N-Hydroxysuccinimidyl benzoate
Benzoic Acid N-Succinimidyl Ester
O-Benzoyl-N,N-succinylhydroxylamine
(2,5-dioxopyrrolidin-1-yl) Benzoate
2,5-Pyrrolidinedione,1-(benzoyloxy)-
benzoic acid N-hydroxysuccinimide ester
BZ-OSU benzoic acid N-hydroxysucciniMide ester
[EINECS(EC#)]

803-576-9
[Molecular Formula]

C11H9NO4
[MDL Number]

MFCD00078953
[MOL File]

23405-15-4.mol
[Molecular Weight]

219.19
Chemical PropertiesBack Directory
[Melting point ]

135.0 to 139.0 °C
[Boiling point ]

342.3±25.0 °C(Predicted)
[density ]

0.68
[storage temp. ]

2-8°C
[form ]

powder to crystal
[color ]

White to Almost white
[InChI]

1S/C11H9NO4/c13-9-6-7-10(14)12(9)16-11(15)8-4-2-1-3-5-8/h1-5H,6-7H2
[InChIKey]

BVUOEDOMUOJKOY-UHFFFAOYSA-N
[SMILES]

O=C1CCC(=O)N1OC(=O)c2ccccc2
Safety DataBack Directory
[Hazard Codes ]

Xi,T
[Risk Statements ]

36/37/38-25
[Safety Statements ]

26-36-45
[RIDADR ]

UN 2811 6.1 / PGIII
[WGK Germany ]

3
[HS Code ]

2925.19.4200
[Storage Class]

6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
[Hazard Classifications]

Acute Tox. 3 Oral
Hazard InformationBack Directory
[Synthesis]

N-Hydroxysuccinimide

6066-82-6

Benzoic acid

65-85-0

BZ-OSU

23405-15-4

GENERAL METHOD: Benzoic acid (0.353 g, 2.89 mmol) was dissolved in 50 mL of anhydrous tetrahydrofuran (THF) and N-hydroxysuccinimide (0.40 g, 3.47 mmol) and N,N'-dicyclohexylcarbodiimide (DCC, 0.776 g, 3.76 mmol) were added in sequence. The reaction mixture was stirred at room temperature for 48 hours. Upon completion of the reaction, the insoluble by-product N,N'-dicyclohexylurea (DCU) was removed by filtration and the filtrate was concentrated under reduced pressure to remove the solvent. The concentrated residue was dissolved in chloroform (CHCl3), the organic phase was dried with anhydrous sodium sulfate (Na2SO4), filtered and the solvent was evaporated to dryness under reduced pressure. The crude product was purified by silica gel column chromatography with the eluent being a hexane solution of 40% ethyl acetate to give the white solid product N-hydroxysuccinimide ester benzoate (0.586 g, 93% yield). To improve the purity of the product, the resulting white solid was recrystallized in 2-propanol.

[References]

[1] Chemical and Pharmaceutical Bulletin, 2007, vol. 55, # 1, p. 124 - 127
[2] Chemistry Letters, 1980, p. 1161 - 1164
[3] Bulletin of the Chemical Society of Japan, 1984, vol. 57, # 3, p. 781 - 786
[4] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 15, p. 4629 - 4632
[5] Journal of the Chemical Society, Chemical Communications, 1985, # 8, p. 473
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