ChemicalBook--->CAS DataBase List--->437655-95-3

437655-95-3

437655-95-3 Structure

437655-95-3 Structure
IdentificationBack Directory
[Name]

5,8,11,14-Tetraoxa-2-azahexadecanedioic acid
[CAS]

437655-95-3
[Synonyms]

Fmoc-PEG4- CH2COOH
Fmoc-NH-PEG4-CH2CO2H
Fmoc-NH-PEG5-CH2CO2H
FMoc-NH-PEG4-CH2COOH
Fmoc-PEG4-acetic acid
5,8,11,14-Tetraoxa-2-azahexadecanedioic acid
1-Hydroxy-1-oxo-5,8,11,14-tetraoxa-2-azahexadecan-16-oic acid
1-(9H-Fluoren-9-yl)-3-oxo-2,7,10,13,16-pentaoxa-4-azaoctadecan-18-oic acid
14-[(9-Fluorenylmethoxycarbonyl)amino]-3,6,9,12-tetraoxatetradecanoic acid
5,8,11,14-Tetraoxa-2-azahexadecanedioic acid 1-(9H-fluoren-9-ylmethyl) ester
14-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-3,6,9,12-tetraoxatetradecanoic acid
[2-(2-{2-[2-((9H-fluoren-9-yl-methoxycarbonyl)amino)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-acetic acid
[Molecular Formula]

C25H31NO8
[MDL Number]

MFCD26142981
[MOL File]

437655-95-3.mol
[Molecular Weight]

473.52
Chemical PropertiesBack Directory
[Melting point ]

51℃
[Boiling point ]

681.3±55.0 °C(Predicted)
[density ]

1.235±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,2-8°C
[form ]

Oil
[pka]

3.39±0.10(Predicted)
[color ]

Colorless to light yellow
[InChI]

InChI=1S/C25H31NO8/c27-24(28)18-33-16-15-32-14-13-31-12-11-30-10-9-26-25(29)34-17-23-21-7-3-1-5-19(21)20-6-2-4-8-22(20)23/h1-8,23H,9-18H2,(H,26,29)(H,27,28)
[InChIKey]

XPNLDOFYRFOXLR-UHFFFAOYSA-N
[SMILES]

C(OCC1C2=C(C=CC=C2)C2=C1C=CC=C2)(=O)NCCOCCOCCOCCOCC(O)=O
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HS Code ]

2942000090
Hazard InformationBack Directory
[Description]

Fmoc-NH-PEG4-CH2COOH is a PEG linker containing an Fmoc-protected amine and a terminal carboxylic acid. The hydrophilic PEG spacer increases solubility in aqueous media. The Fmoc group can be deprotected under basic condition to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can react with primary amine groups in the presence of activators (e.g. EDC, or HATU) to form a stable amide bond.
[Biological Activity]

Fmoc-NH-PEG4-CH2COOH is a degradable ADC linker for antibody drug conjugate (ADC) synthesis. It is also a PEG-based PROTAC linker, which can be used for PROTAC synthesis.
[Synthesis]

Amino-PEG4-CH2CO2H

195071-49-9

(9H-fluoren-9-yl)methyl 2,5-dioxopyrrolidine-1-carboxylate

102774-86-7

5,8,11,14-Tetraoxa-2-azahexadecanedioic acid

437655-95-3

The general procedure for the synthesis of 1-(9H-fluoren-9-yl)-3-oxo-2,7,10,13,16-pentaoxa-4-azaoctadecan-18-oic acid from 14-amino-3,6,9,12-tetraoxatetradecane-1-oic acid and compounds (CAS: 102774-86-7) was as follows: 14-amino-3,6,9,12-tetraoxatetradecane -1-acid (0.79 g, 3.14 mmol) and K2CO3 (1.04 g, 7.50 mmol) were dissolved in 5.8 mL of water and stirred at room temperature for 15 minutes. Subsequently, N-(9-fluorenylmethoxycarbonyl)succinimide (Fmoc-OSu, 1.28 g, 3.79 mmol) was added, and stirring of the reaction mixture was continued for 24 h, during which the reaction progress was monitored by thin-layer chromatography (TLC, with unfolding agent ratio of CHCl3/MeOH/AcOH, 5:1:0.06). Upon completion of the reaction, the salts were removed by filtration and the filtrate was washed with ether (Et2O) and then acidified with 3N hydrochloric acid to pH 1. The acidified solution was used to extract the target compounds with dichloromethane (DCM). After the extraction was completed, the solvent was removed by distillation under reduced pressure and the resulting crude product was purified by reversed-phase high performance liquid chromatography (RP-HPLC). The fraction containing the target product was collected and lyophilized to give compound 11a (1.08 g, 73% yield). Compound 11a has the chemical formula C25H11NO8, theoretical mass-to-charge ratio [M + H]+ = 474.2, measured mass-to-charge ratio [M + H]+ = 474.9, [M + Na]+ = 496.9.

[in vitro]

ADCs are comprised of an antibody to which is attached an ADC cytotoxin through an ADC linker.
PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins.

[target]

Cleavable

Alkyl/ether

PEGs

[References]

[1] Patent: US2018/169262, 2018, A1. Location in patent: Paragraph 0181-0183
Spectrum DetailBack Directory
[Spectrum Detail]

5,8,11,14-Tetraoxa-2-azahexadecanedioic acid(437655-95-3)1HNMR
437655-95-3 suppliers list
Company Name: Yaopu(Shanghai) Pharmaceutical Technology Co., Ltd  Gold
Telephone: 50929289 18616309303
Website: www.ypptech.com.cn
Company Name: Shanghai Huici Pharmaceutical Technology Co., LTD  Gold
Telephone: 133-31922809 19372841038
Website: http://www.pharmahuici.com
Company Name: Jinan Junhe Pharmaceutical Co., Ltd  Gold
Telephone: +86-13053355392 +86-13053355392
Website: www.chemicalbook.com/supplier/25201904/
Company Name: Chengdu Pukang Biotechnology Co., Ltd  
Telephone: 18217049878
Website: www.peglinke.com
Company Name: T&W GROUP  
Telephone: 021-61551611 13296011611
Website: www.trustwe.com/
Company Name: Shanghai Aladdin Bio-Chem Technology Co.,LTD  
Telephone: 400-6206333 13167063860
Website: www.aladdin-e.com/
Company Name: The future of Shanghai Industrial Co., Ltd.  
Telephone: 021-61552785
Website: www.jonln.com
Company Name: Nanjing Junnahe Biopharmaceutical Co., Ltd  
Telephone: 025-58367986 17351780683
Website: https://www.chemicalbook.com/productlist.aspx?cbn=CB0386760
Company Name: TargetMol Chemicals Inc.  
Telephone: 021-021-33632979 15002134094
Website: https://www.targetmol.cn/
Company Name: Shanghai JONLN Reagent Co., Ltd.  
Telephone: 400-0066400 13621662912
Website: http://www.jonln.com
Company Name: Bide Pharmatech Ltd.  
Telephone: 400-164-7117 18317119277
Website: www.bidepharm.com
Company Name: Hunan HuaTeng Pharmaceutical Co., Ltd.,  
Telephone: 400-8592883 15367835770
Website: www.huatengsci.com
Company Name: Shanghai Boka-chem Tech. Inc.  
Telephone: 400-026-1533/(021) 6478-0600
Website: www.bokachem.com
Company Name: Credit Asia Chemical Co., Ltd.  
Telephone: +86 (21) 61124340
Website: www.chemicalbook.com/ShowSupplierProductsList16523/0_EN.htm
Company Name: AN PharmaTech Co Ltd  
Telephone: 86(21)68097365
Website: www.anpharma.net
Company Name: Tongling HengYou Biotechnology Co., Ltd.  
Telephone: 021-50426030 13856289449;13124863828
Website: www.chemicalbook.com/ShowSupplierProductsList16800/0_EN.htm
Company Name: Tianjing Geneston Bio-tech Co.,Ltd.  
Telephone: 022-60131465 18920720807
Website: https://www.chemicalbook.com/ShowSupplierProductsList16827/0_EN.htm
Company Name: Borenpharm Co., Ltd  
Telephone: 027-65563561
Website: www.borenpharm.com
Tags:437655-95-3 Related Product Information
72040-63-2 74654-07-2 581065-95-4 25990-96-9 651042-83-0 756525-99-2 756525-92-5 2615-15-8 635287-26-2 892154-71-1 581066-04-8 4437-01-8 557756-85-1 359860-27-8 52190-55-3 72236-26-1 2101563-45-3 1863885-74-8