m-PEG2-Tos - ≥95% , CAS No.50586-80-6

CAS: 50586-80-6 Cat. No.: M412483 분자식: C₁₂H₁₈O₅S 분자량: 274.34 EC 번호: 633-362-9

GRADE & PURITY ≥95%

Synonyms

2-(2-methoxy-ethoxy)ethyl 4-toluenesulfonate | 2-(2-methoxyethoxy)ethyl 4-toluenesulfonate | HY-42745 | 1-methyl -L-tryptophan | m-PEG2-Tos | 2,6-dichlor-4-methylpyridin-3-carboxylic acid | SCHEMBL361530 | AS-69959 | 2-(2-methoxyethoxy)ethyl tosylate | m-

Storage

Store at -20°C

Shipped In

Ice chest + Ice pads

Application

Antibody Drug Conjugates(ADC), Drug Delivery, Surface Modification, PEGylation of Protein, Peptide & Oligo

개요

Information

m-PEG2-Tos is an uncleavable ADC linker applied into the synthesis of antibody-drug conjugates (ADCs).

Specifications

동의어

2-(2-methoxy-ethoxy)ethyl 4-toluenesulfonate | 2-(2-methoxyethoxy)ethyl 4-toluenesulfonate | HY-42745 | 1-methyl -L-tryptophan | m-PEG2-Tos | 2,6-dichlor-4-methylpyridin-3-carboxylic acid | SCHEMBL361530 | AS-69959 | 2-(2-methoxyethoxy)ethyl tosylate | m-

사양 및 순도

≥95%

생화학 및 생리적 메커니즘

m-PEG2-Tos is an uncleavable ADC linker applied into the synthesis of antibody-drug conjugates (ADCs).

보관 조건

Store at -20°C

배송

Ice chest + Ice pads

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순수함

≥95%

이름과 식별자

• Pubchem Sid: 508811247
• 정식 스마일: CC1=CC=C(C=C1)S(=O)(=O)OCCOCCOC
• IUPAC Name: 2-(2-methoxyethoxy)ethyl 4-methylbenzenesulfonate
• InChIKey: PBKGNJXLJQARIN-UHFFFAOYSA-N
• INCHI: 1S/C12H18O5S/c1-11-3-5-12(6-4-11)18(13,14)17-10-9-16-8-7-15-2/h3-6H,7-10H2,1-2H3
• 이성체 SMILES: CC1=CC=C(C=C1)S(=O)(=O)OCCOCCOC
• 분자량: 274.34
• Reaxy-Rn: 2863313
• Reaxys-RN_link_address: https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2863313&ln=

Taxonomic Classification

Taxonomy Tree

• Kingdom Organic compounds
  • Superclass Benzenoids
    • 분류 Benzene and substituted derivatives
      • Subclass Benzenesulfonic acids and derivatives

• Kingdom: Organic compounds
• Superclass: Benzenoids
• 분류: Benzene and substituted derivatives
• Subclass: Benzenesulfonic acids and derivatives
• Intermediate Tree Nodes: Not available
• Direct Parent: Benzenesulfonate esters
• Alternative Parents: p-Methylbenzenesulfonates Tosyl compounds Benzenesulfonyl compounds Arylsulfonic acids and derivatives Organosulfonic acid esters Sulfonyls Dialkyl ethers Organic oxides Hydrocarbon derivatives
• Molecular Framework: Aromatic homomonocyclic compounds
• Substituents: Benzenesulfonate ester - P-methylbenzenesulfonate - Tosyl compound - Arylsulfonic acid or derivatives - Benzenesulfonyl group - Toluene - Organosulfonic acid ester - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Dialkyl ether - Ether - Organic oxygen compound - Organosulfur compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Aromatic homomonocyclic compound
• 설명: This compound belongs to the class of organic compounds known as benzenesulfonate esters. These are arenesulfonate esters that result from the formal condensation of the hydroxy group of an alcohol, enol, phenol or heteroarenol with benzenesulfonic acid.
• 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

화학 및 물리적 특성

• 용해성: Solubility (25°C) In vitro
• 발화점(°C): 191 °C
• 분자량: 274.340 g/mol
• XLogP3: 1.100
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 5
• Rotatable Bond Count: 8
• Exact Mass: 274.087 Da
• Monoisotopic Mass: 274.087 Da
• Topological Polar Surface Area: 70.200 Ų
• Heavy Atom Count: 18
• Formal Charge: 0
• Complexity: 301.000
• 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