CAS 212783-75-0
:2-[[5-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-2-yl]oxy]acetic acid
Description:
The chemical substance known as 2-[[5-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-2-yl]oxy]acetic acid, with the CAS number 212783-75-0, is a complex organic compound characterized by its unique structural features. It contains a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is commonly used in peptide synthesis to protect amino groups. The compound also features a dibenzo[a,d]cycloheptene moiety, contributing to its potential biological activity. The presence of the acetic acid functional group indicates that it has acidic properties, which may influence its solubility and reactivity in various environments. This substance is likely to be of interest in medicinal chemistry and drug development due to its intricate structure, which may interact with biological targets. Its synthesis and characterization would typically involve advanced organic chemistry techniques, and it may be utilized in research related to peptide synthesis or as a building block in the development of pharmaceuticals.
Formula:C32H27NO5
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)
InChI key:InChIKey=XHOBPBDZGGKEOX-UHFFFAOYSA-N
SMILES:C(OC(NC1C=2C(=CC(OCC(O)=O)=CC2)CCC=3C1=CC=CC3)=O)C4C=5C(C=6C4=CC=CC6)=CC=CC5
Synonyms:- (R,S)-2-[[5-(9-Fluorenylmethyloxycarbonylamino)-dibenzo[a,d]cycloheptane-2-yl]oxy]acetic acid
- 2-((5-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-10,11-dihydro-5H-dibenzo[a,d][7]annulen-2-yl)oxy)acetic acid
- 2-[[5-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-2-yl]oxy]acetic acid
- 2-{[(R,S)-5-(9-Fluorenylmethyloxycarbonyl-amino)-10, 11-dihydro-5H-dibenzo[a,d]cycloheptene-2-yl]oxy}acetic acid
- Acetic acid, 2-[[5-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-2-yl]oxy]-
- Acetic acid, [[5-[[(9H-fluoren-9-ylmethoxy)carbonyl]amino]-10,11-dihydro-5H-dibenzo[a,d]cyclohepten-2-yl]oxy]-
- Fmoc-Suberol
- [(5-{[(9H-fluoren-9-ylmethoxy)carbonyl]amino}-10,11-dihydro-5H-dibenzo[a,d][7]annulen-2-yl)oxy]acetic acid
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Found 6 products.
Fmoc-Suberol
CAS:A linker suitable for Fmoc-SPPS of peptide amides. Cleavage is achieved e.g. with 95% TFA, scavengers may be required.Formula:C32H27NO5Purity:98.5%Color and Shape:WhitishMolecular weight:505.572-((5-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-10,11-dihydro-5H-dibenzo[a,d][7]annulen-2-yl)oxy)acetic acid
CAS:Formula:C32H27NO5Purity:96%Color and Shape:SolidMolecular weight:505.56052-((5-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-10,11-dihydro-5H-dibenzo[a,d][7]annulen-2-yl)oxy)acetic acid
CAS:2-((5-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-10,11-dihydro-5H-dibenzo[a,d][7]annulen-2-yl)oxy)acetic acidPurity:96%Molecular weight:505.56g/molRamage linker
CAS:<p>Ramage Linker,Fmoc-Suberol is a synthetic derivative of the antimicrobial peptide guanylate. It is used as an inhibitor of congestive heart failure. Ramage Linker,Fmoc-Suberol has been shown to be effective in reducing the severity of congestive heart failure by inhibiting the production of brain natriuretic peptides. The chemical structure and sequence have been determined using a combination of structural analysis and degradable linkers that are cleaved in vivo by hydrolysis or enzymatic degradation. Ramage Linker,Fmoc-Suberol has also been shown to reduce blood pressure and inhibit platelet aggregation.</p>Formula:C32H27NO5Purity:Min. 95%Color and Shape:PowderMolecular weight:505.56 g/molRamage Linker (FMOC-Suberol) extrapure, 98%
CAS:Formula:C32H27NO5Purity:min. 98%Color and Shape:White to off white, Crystalline powderMolecular weight:505.58





