Succinimide - ≥99% , CAS No.123-56-8

CAS: 123-56-8 Cat. No.: S104079 Peso molecular: 99.09 Beilstein Registry Number: 108440 Número EC: 204-635-6 PubChem CID: 11439

GRADE & PURITY ≥99%

Synonyms

DB13376 | NSC 11204 | 3,4-Dihydropyrrolidine | BDBM7814 | Q419430 | pyrroldine-2,5-dione | 1BBF5533-77F1-4B20-96F3-0BB022C36CD3 | DTXCID3030181 | NSC13114 | NSC-13114 | SUCCIMIDE | Succinic imide | SUCCINIMIDE | Succinimide pharbiol (TN) | WLN: T5VMVTJ |

Storage

Store at 2-8°C

Shipped In

Wet ice

Specifications

Sinónimos

DB13376 | NSC 11204 | 3, 4-Dihydropyrrolidine | BDBM7814 | Q419430 | pyrroldine-2, 5-dione | 1BBF5533-77F1-4B20-96F3-0BB022C36CD3 | DTXCID3030181 | NSC13114 | NSC-13114 | SUCCIMIDE | Succinic imide | SUCCINIMIDE | Succinimide pharbiol (TN) | WLN: T5VMVTJ |

Especificaciones y pureza

≥99%

Condiciones de almacenamiento de almacenamiento

Store at 2-8°C

Enviado en

Wet ice

Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.

Pureza

≥99%

Nombres e identificadores

• Pubchem Sid: 504752123
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504752123
• Sonrisas canónicas: C1CC(=O)NC1=O
• IUPAC Name: pyrrolidine-2,5-dione
• InChIKey: KZNICNPSHKQLFF-UHFFFAOYSA-N
• INCHI: 1S/C4H5NO2/c6-3-1-2-4(7)5-3/h1-2H2,(H,5,6,7)
• Isómeros SMILES: C1CC(=O)NC1=O
• WGK Alemania: 2
• RTECS: WN2200000
• PubChem CID: 11439
• Peso molecular: 99.09
• Beilstein: 108440

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Organoheterocyclic compounds
    • Clase Pyrrolidines
      • Subclass Pyrrolidones

• Kingdom: Organic compounds
• Superclass: Organoheterocyclic compounds
• Clase: Pyrrolidines
• Subclass: Pyrrolidones
• Intermediate Tree Nodes: Not available
• Direct Parent: Pyrrolidine-2-ones
• Alternative Parents: N-unsubstituted carboxylic acid imides Dicarboximides Lactams Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aliphatic heteromonocyclic compounds
• Substituents: 2-pyrrolidone - Carboxylic acid imide - Dicarboximide - Carboxylic acid imide, n-unsubstituted - Lactam - Carboxylic acid derivative - Azacycle - Carbonyl group - Organooxygen compound - Organonitrogen compound - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aliphatic heteromonocyclic compound
• Descripción: This compound belongs to the class of organic compounds known as pyrrolidine-2-ones. These are pyrrolidines which bear a C=O group at position 2 of the pyrrolidine ring.
• External Descriptors: a small molecule

Data sources

1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.

DOI: 10.1186/s13321-016-0174-y

Objetivos asociados (humanos)

GSK3A Tclin Glycogen synthase kinase-3 (736 Activities)

Discover Target: GSK3A

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Objetivos asociados (no humanos)

Mus musculus (284745 Activities)

Explore this target

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Rattus norvegicus (775804 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Heart (171 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Cereblon isoform 4 (52 Activities)

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Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

Mecanismos de acción

Propiedades químicas y físicas

• Solubilidad: Soluble in water and ethanol. Insoluble in ether and chloroform.
• Sensibilidad: heat sensitive
• Punto de inflamación (°F): 393°F
• Punto de inflamación (°C): 201℃
• Punto de ebullición (°C): 285-290°C
• Punto de fusión (°C): 123-125°C
• Peso molecular: 99.090 g/mol
• XLogP3: -1.000
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 0
• Exact Mass: 99.032 Da
• Monoisotopic Mass: 99.032 Da
• Topological Polar Surface Area: 46.200 Ų
• Heavy Atom Count: 7
• Formal Charge: 0
• Complexity: 105.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 0
• Undefined Atom Stereocenter Count: 0
• Defined Bond Stereocenter Count: 0
• Undefined Bond Stereocenter Count: 0
• The total count of all stereochemical bonds: 0
• Covalently-Bonded Unit Count: 1

Referencias

1. Jiqing Dong, Ran Ping, Xun Dai, Dongchao Wang, Fusheng Liu, Shanshan Du, Mengshuai Liu.  (2022)  Pyrrolidine-2,5-dione-derived ionic liquids promoted efficient transformation of flue gas CO2 into α-alkylidene cyclic carbonates at room temperature.  Journal of CO2 Utilization,      [PMID:] [10.1016/j.jcou.2022.102227]

2. Fan Ye, Liwei Shen, Shi Liu, Huanyu Liu, Xinyuan Zhang, Zejun Zhang, Ying Yang, Xuening Feng, Yuqi Tang, Dong Xiang, Yuanzhu Mi, Xuemin Yan.  (2022)  Demulsification of amphiphilic gemini ionic liquids and its demulsification mechanism.  CHEMOSPHERE,      [PMID:36181854] [10.1016/j.chemosphere.2022.136650]

3. Mengnan Li, Jinling Wang, Xiaoyong Xu, Guobin Ren, Bin Zhu, Minghuang Hong, Zhong Li.  (2022)  Study of Cycloxaprid Co-crystals: Characterization, Theory Calculation, Solubility, and Stability.  CRYSTAL GROWTH & DESIGN,      [PMID:] [10.1021/acs.cgd.2c00394]

4. Wenjuan Fang, Fei Xu, Yaqin Zhang, Heng Wang, Zhencai Zhang, Zifeng Yang, Weiwei Wang, Hongyan He, Yunjun Luo.  (2021)  Acylamido-based anion-functionalized ionic liquids for efficient synthesis of poly(isosorbide carbonate).  Catalysis Science & Technology,  12  (6): (1756-1765).  [PMID:] [10.1039/D1CY01824H]

5. Wen jie Kuang, Shao chang Ji, Shen min Xu, Ping Lan, An ping Liao, Ju ying Zhou, Jin yan Zhang.  (2019)  Thermodynamic and Crystallization of Lamotrigine Cocrystal.  CRYSTAL GROWTH & DESIGN,      [PMID:] [10.1021/acs.cgd.9b01028]

6. Yan Liu, Huiyuan Hu, Xinlin Yang, Jing Lv, Li Zhou, Zhongkuan Luo.  (2019)  Hydrophilic modification on polyvinyl alcohol membrane by hyaluronic acid.  Biomedical Materials,  14  (5): (055009).  [PMID:31284277] [10.1088/1748-605X/ab3010]

7. Wentao Zheng, Jialing Chen, Yujiao Jia, Nengqi Sun, Xiankun Wu.  (2025)  Thermodynamic analysis of nitric oxide absorption in deep eutectic solvents comprising 1,1,3,3-tetramethylguanidine.  JOURNAL OF CHEMICAL THERMODYNAMICS,      [PMID:] [10.1016/j.jct.2025.107563]

8. Qi Tan, Zhiwei Liu, Yao Zhang, Yongle Xia, Xiaoyi Zhang, Bingliang Gao.  (2025)  Superbase-alcohol vitreous mixture solvents containing additives for efficient and reversible CO2 capture.  Journal of Environmental Chemical Engineering,      [PMID:] [10.1016/j.jece.2025.119114]