[(5-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-10,11-dihydro-5H-dibenzo[a,d][7]annulen-2-yl)oxy]acetic acid | CAS No. 212783-75-0

[(5-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-10,11-dihydro-5H-dibenzo[a,d][7]annulen-2-yl)oxy]acetic acid

Basic Information

CAS Number

212783-75-0

Molecular Formula

C32H27NO5

Molecular Weight

505.57 g/mol

AD

Basic Physical Properties

C1CC2=C(C=CC(=C2)OCC(=O)O)C(C3=CC=CC=C31)NC(=O)OCC4C5=CC=CC=C5C6=CC=CC=C46

InChI

InChI=1S/C32H27NO5/c34-30(35)19-37-22-15-16-24-21(17-22)14-13-20-7-1-2-8-23(20)31(24)33-32(36)38-18-29-27-11-5-3-9-25(27)26-10-4-6-12-28(26)29/h1-12,15-17,29,31H,13-14,18-19H2,(H,33,36)(H,34,35)

InChIKey

XHOBPBDZGGKEOX-UHFFFAOYSA-N

LogP

5.876700000000005

Topological Polar Surface Area

84.86000000000001 Ų

Hydrogen Bond Donor/Acceptor

2 / 6

Complexity

811

Synonyms & References

English

  • MFCD07783960
  • Ramage-Linker
  • ACETIC ACID, 2-[[5-[[(9H-FLUOREN-9-YLMETHOXY)CARBONYL]AMINO]-10,11-DIHYDRO-5H-DIBENZO[A,D]CYCLOHEPTEN-2-YL]OXY]-
  • FMOC-SUBEROL, Ramage Linker
  • 2-[[2-(9H-fluoren-9-ylmethoxycarbonylamino)-6-tricyclo[9.4.0.03,8]pentadeca-1(15),3(8),4,6,11,13-hexaenyl]oxy]acetic acid
  • J-013969
  • AKOS015920104
  • Ramage Linker, Fmoc Suberol
  • BCP16052
  • DTXSID901108676
  • CS-W009750
  • 2-[[5-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-2-yl]oxy]acetic acid
  • AMY22695
  • 212783-75-0
  • SCHEMBL22572694
  • 2-((5-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-10,11-dihydro-5H-dibenzo[a,d][7]annulen-2-yl)oxy)acetic acid
  • Ramage Linker
  • 2-((5-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-10,11-dihydro-5H-dibenzo[a,d][7]annulen-2-yl)oxy)aceticacid
  • FT-0643964
  • HY-W009034
  • 5-Fmoc-Amino-10, 11-Dihydro-5H-Dibenzo[a,d]Cycloheptene-2-Hydroxy Acetic Acid
  • AC-32003
  • FMOC-SUBEROL
  • CS-17334
  • Ramagelinker
  • (R,S)-2-[[5-(9-Fluorenylmethyloxycarbonylamino)-dibenzo[a,d]cycloheptane-2-yl]oxy]acetic acid
  • Fmoc-Suberol
  • Ramage Linker(Fmoc-Suberol)
  • RAMAGE LINKER, FMOC-SUBEROL, 2-{[(R,S)-5-(9-FLUORENYLMETHYLOXYCARBONYL-AMINO)-10,11-DIHYDRO-5H-DIBENZO[A,D]CYCLOHEPTENE...
  • Ramage LinkerFmoc-Sub
  • (R,S)-2-[[5-(9-FLUORENYLMETHYLOXYCARBONYLAMINO)-DIBENZO[A,D]CYCLOHEPTANE-2-YL]OXY]-ACETIC ACID

MDL Number

MFCD07783960

FAQ

What are the physical and chemical properties of [(5-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-10,11-dihydro-5H-dibenzo[a,d][7]annulen-2-yl)oxy]acetic acid (CAS: 212783-75-0)?

The compound [(5-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-10,11-dihydro-5H-dibenzo[a,d][7]annulen-2-yl)oxy]acetic acid (CAS: 212783-75-0) is a crystalline solid with a molecular weight of approximately 690 g/mol. It is poorly soluble in water but soluble in organic solvents like DMSO and DMF. The compound is reactive towards nucleophiles and exhibits stability under mild conditions. It is used as a building block in organic synthesis and drug development.

How is [(5-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-10,11-dihydro-5H-dibenzo[a,d][7]annulen-2-yl)oxy]acetic acid (CAS: 212783-75-0) typically synthesized?

The compound is typically synthesized via multistep organic reactions starting from fluorenylmethanol and 2-aminobenzaldehyde. The synthesis involves protection, coupling, and deprotection steps using standard reagents and conditions. The final product is obtained with a yield of around 70-80%.

What industries use [(5-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-10,11-dihydro-5H-dibenzo[a,d][7]annulen-2-yl)oxy]acetic acid (CAS: 212783-75-0)?

This compound is primarily used in the pharmaceutical and biotechnology industries for drug development and as a precursor in organic synthesis. It is also explored in the polymer and materials science sectors for its unique chemical properties.

What precautions should be taken when handling [(5-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-10,11-dihydro-5H-dibenzo[a,d][7]annulen-2-yl)oxy]acetic acid (CAS: 212783-75-0)?

When handling [(5-{[(9H-Fluoren-9-ylmethoxy)carbonyl]amino}-10,11-dihydro-5H-dibenzo[a,d][7]annulen-2-yl)oxy]acetic acid (CAS: 212783-75-0), ensure the use of personal protective equipment (PPE) including gloves, goggles, and a lab coat. Work in a fume hood to minimize exposure. Dispose of any waste according to local regulations and consult the Safety Data Sheet (SDS) for detailed handling instructions.

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