N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-[4-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)butyl]glycine | CAS No. 171856-09-0

N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-[4-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)butyl]glycine

Basic Information

CAS Number

171856-09-0

Molecular Formula

C26H32N2O6

Molecular Weight

468.55 g/mol

AD

Basic Physical Properties

CC(C)(C)OC(=O)NCCCCN(CC(=O)O)C(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13

InChI

InChI=1S/C26H32N2O6/c1-26(2,3)34-24(31)27-14-8-9-15-28(16-23(29)30)25(32)33-17-22-20-12-6-4-10-18(20)19-11-5-7-13-21(19)22/h4-7,10-13,22H,8-9,14-17H2,1-3H3,(H,27,31)(H,29,30)

InChIKey

MNAXPVXIHALBEF-UHFFFAOYSA-N

LogP

4.627000000000004

Topological Polar Surface Area

105.17 Ų

Hydrogen Bond Donor/Acceptor

2 / 8

Complexity

684

Safety Information

View Safety Information

GHS Hazard Pictograms

H410H410

Hazard Statement

H410 Very toxic to aquatic life with long lasting effects
Hazardous to the aquatic environment, long-term hazard

Synonyms & References

English

  • J-010768
  • CS-0201699
  • 2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(4-((tert-butoxycarbonyl)amino)butyl)amino)acetic acid
  • Fmoc-N-(4-Boc-aminobutyl)glycine
  • MNAXPVXIHALBEF-UHFFFAOYSA-N
  • 2-((((9H-fluoren-9-yl)methoxy)carbonyl)(4-(tert-butoxycarbonylamino)butyl)amino)acetic acid
  • Fmoc-{Boc-NH(CH2)4}Gly-OH
  • 2-[9H-fluoren-9-ylmethoxycarbonyl-[4-[(2-methylpropan-2-yl)oxycarbonylamino]butyl]amino]acetic acid
  • Fmoc-Abg(Boc)-OH
  • FT-0701226
  • AKOS015911531
  • Fmoc-N-(4-Boc-aminobutyl)-Gly-OH
  • [(4-tert-Butoxycarbonylamino-butyl)-(9H-fluoren-9-ylmethoxycarbonyl)-amino]-acetic acid
  • SCHEMBL4599714
  • N-(9-Fluorenylmethyloxycarbonyl)-N-[4-(t-butyloxycarbonylamino)butyl]-glycine
  • N-[4-(Boc-amino)butyl]-N-Fmoc-glycine
  • 2-[(4-{[(tert-butoxy)carbonyl]amino}butyl)({[(9H-fluoren-9-yl)methoxy]carbonyl})amino]acetic acid
  • DTXSID70373278
  • 171856-09-0
  • N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N-(4-((tert-butoxycarbonyl)amino)butyl)glycine
  • Glycine,N-[4-[[(1,1-dimethylethoxy)carbonyl]amino]butyl]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-
  • MFCD04112689
  • E70683
  • AS-81598
  • HY-W141907
  • Fmoc-N-(4-Boc-aminobutyl)-Gly-OH, >=98.0% (HPLC)
  • Fmoc-abg(boc)-oh
  • FMOC-N-(4-BOC-AMINOBUTYL)GLYCINE,
  • AC1MBSYF
  • CTK8F0790
  • Fmoc-Nlys(Boc)-OH

MDL Number

MFCD04112689

Customs Code

29242990

FAQ

What are the physical and chemical properties of N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-[4-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)butyl]glycine (CAS: 171856-09-0)?

This compound is a crystalline solid with a molecular weight of approximately 610.55 g/mol. It has limited water solubility and is highly reactive, particularly with bases. It is stable under normal conditions but should be protected from moisture. Reactivity is enhanced in basic conditions, making it suitable for peptide coupling reactions.

How is N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-[4-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)butyl]glycine (CAS: 171856-09-0) typically synthesized?

The compound is synthesized through a multi-step process involving fluorenylmethyloxycarbonyl (Fmoc) protection, followed by amidation and acylation reactions. Commonly, the Fmoc group is introduced using Fluorenylmethoxycarbonyl chloride (Fmoc-Cl), and the product is purified by column chromatography. This process requires careful control of pH and temperature to ensure high yield and selectivity.

What industries use N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-[4-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)butyl]glycine (CAS: 171856-09-0)?

This compound is primarily used in pharmaceuticals, where it serves as an intermediate in the synthesis of complex peptides and proteins. It is also utilized in polymer science for the modification of polymers and in semiconductor manufacturing for specific surface chemistry applications.

What precautions should be taken when handling N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-[4-({[(2-methyl-2-propanyl)oxy]carbonyl}amino)butyl]glycine (CAS: 171856-09-0)?

When handling this compound, it is essential to wear appropriate personal protective equipment (PPE), including gloves, goggles, and lab coat. Work should be conducted in a well-ventilated area or fume hood to avoid inhalation. Spills should be cleaned up carefully using appropriate safety measures, and the Material Safety Data Sheet (MSDS) should be consulted for detailed handling instructions.

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