Fmoc-Ser-OH - ≥97% , CAS No.73724-45-5

CAS: 73724-45-5 Cat. No.: F103020 Peso molecular: 327.33 Beilstein Registry Number: 4715791 Número EC: 690-938-2

GRADE & PURITY ≥97%

Synonyms

AC-26241 | Fmoc-L-Ser-OH | Fmoc-Ser-OH H2O | SCHEMBL118370 | (((9H-Fluoren-9-yl)methoxy)carbonyl)-L-serine | (2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-hydroxypropanoic acid | N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-L-SERINE | Fmoc-Ser-OH H | JZT

Storage

Conservar a 2-8°C

Shipped In

Hielo húmedo

Specifications

Sinónimos

AC-26241 | Fmoc-L-Ser-OH | Fmoc-Ser-OH H2O | SCHEMBL118370 | (((9H-Fluoren-9-yl)methoxy)carbonyl)-L-serine | (2S)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3-hydroxypropanoic acid | N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-L-SERINE | Fmoc-Ser-OH H | JZT

Especificaciones y pureza

≥97%

Condiciones de almacenamiento de almacenamiento

Conservar a 2-8°C

Enviado en

Hielo húmedo

Pureza

≥97%

Nombres e identificadores

• Pubchem Sid: 504764278
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504764278
• Sonrisas canónicas: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CO)C(=O)O
• IUPAC Name: (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-hydroxypropanoic acid
• InChIKey: JZTKZVJMSCONAK-INIZCTEOSA-N
• INCHI: 1S/C18H17NO5/c20-9-16(17(21)22)19-18(23)24-10-15-13-7-3-1-5-11(13)12-6-2-4-8-14(12)15/h1-8,15-16,20H,9-10H2,(H,19,23)(H,21,22)/t16-/m0/s1
• Isómeros SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)N[C@@H](CO)C(=O)O
• WGK Alemania: 3
• Peso molecular: 327.33
• Beilstein: 4715791
• Reaxy-Rn: 7170699
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7170699&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • Clase Fluorenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Clase: Fluorenes
• Subclass: Not available
• Intermediate Tree Nodes: Not available
• Direct Parent: Fluorenes
• Alternative Parents: Serine and derivatives Beta hydroxy acids and derivatives Carbamate esters Organic carbonic acids and derivatives Monocarboxylic acids and derivatives Carboxylic acids Primary alcohols Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
• Molecular Framework: Aromatic homopolycyclic compounds
• Substituents: Fluorene - Serine or derivatives - Alpha-amino acid or derivatives - Beta-hydroxy acid - Hydroxy acid - Carbamic acid ester - Carbonic acid derivative - Monocarboxylic acid or derivatives - Carboxylic acid - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Organonitrogen compound - Carbonyl group - Alcohol - Aromatic homopolycyclic compound
• Descripción: This compound belongs to the class of organic compounds known as fluorenes. These are compounds containing a fluorene moiety, which consists of two benzene rings connected through either a cyclopentane, cyclopentene, or cyclopenta-1,3-diene.
• External Descriptors: Not available

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

Propiedades químicas y físicas

• Solubilidad: Soluble in Methanol
• Rotación específica [α]: -12.5 ° (C=1, DMF)
• Punto de fusión (°C): 102-106°C
• Peso molecular: 327.300 g/mol
• XLogP3: 2.000
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 6
• Exact Mass: 327.111 Da
• Monoisotopic Mass: 327.111 Da
• Topological Polar Surface Area: 95.900 Ų
• Heavy Atom Count: 24
• Formal Charge: 0
• Complexity: 446.000
• Isotope Atom Count: 0
• Defined Atom Stereocenter Count: 1
• 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. Zhanpeng Ren, Jianying Wang, Chenglong Xue, Minghua Deng, Haiyang Yu, Tianci Lin, Jiayuan Zheng, Rongxiang He, Xianbao Wang, Jinhua Li.  (2023)  Ultrahighly Sensitive and Selective Glutathione Sensor Based on Carbon Dot-Functionalized Solution-Gate Graphene Transistor.  ANALYTICAL CHEMISTRY,      [PMID:37971943] [10.1021/acs.analchem.3c03656]

2. Cong Huang, Zhuang Hao, Ziran Wang, Hao Wang, Xuezeng Zhao, Yunlu Pan.  (2022)  An Ultraflexible and Transparent Graphene-Based Wearable Sensor for Biofluid Biomarkers Detection.  Advanced Materials Technologies,  7  (6): (2101131).  [PMID:] [10.1002/admt.202101131]

3. Xianlin Xu, Guodong Zhao, Hang Wang, Xiaojie Li, Xi Feng, Bowen Cheng, Lei Shi, Weimin Kang, Xupin Zhuang, Yan Yin.  (2018)  Bio-inspired amino-acid-functionalized cellulose whiskers incorporated into sulfonated polysulfone for proton exchange membrane.  JOURNAL OF POWER SOURCES,      [PMID:] [10.1016/j.jpowsour.2018.11.003]