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

CAS: 73724-45-5 Cat. No.: F103020 Molecular Weight: 327.33 Beilstein Registry Number: 4715791 EC Number: 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

Store at 2-8°C

Shipped In

Wet ice

Specifications

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

Specifications & Purity

≥97%

Storage

Store at 2-8°C

Shipped In

Wet ice

This product requires cold chain shipping. Ground and other economy services are not available.

Purity

≥97%

Names and Identifiers

• Pubchem Sid: 504764278
• Pubchem Sid Url: https://pubchem.ncbi.nlm.nih.gov/substance/504764278
• Canonical Smiles: 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
• Isomeric SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)N[C@@H](CO)C(=O)O
• WGK Germany: 3
• Molecular Weight: 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
    • Class Fluorenes

• Kingdom: Organic compounds
• Superclass: Benzenoids
• Class: 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
• Description: 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

Chemical and Physical Properties

• Solubility: Soluble in Methanol
• Specific Rotation[α]: -12.5 ° (C=1, DMF)
• Melt Point(°C): 102-106°C
• Molecular Weight: 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

References

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]