ChemicalBook > Product Catalog >Biochemical Engineering >Amino Acids and Derivatives >Aspartic acid derivatives >FMOC-ASP(ODMAB)-OH

FMOC-ASP(ODMAB)-OH

FMOC-ASP(ODMAB)-OH Structure
CAS No.
269066-08-2
Chemical Name:
FMOC-ASP(ODMAB)-OH
Synonyms
Fomc-Asp(Odmab)-OH;FMOC-ASP(ODMAB)-OH;Fmoc-L-Asp(ODmab)-OH;FMOC-ASPARTIC ACID(ODMAB);FMOC-ASP(ODMAB)-OH USP/EP/BP;(9H-Fluoren-9-yl)MethOxy]Carbonyl Asp(ODMAB)-OH;FMoc-L-aspartic acid b-4-[N-{1-(4,4-diMethyl-2,6-dioxocyclohexylidene)-3-Methylbutyl}aMino]benzyl ester;Fmoc-L-aspartic acid β-4-[N-{1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl}amino]benzyl ester;Fmoc-L-aspartic acid beta-4-[N-{1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl}amino]benzyl ester;FMOC-L-ASPARTIC ACID BETA-4-[N-[1-(4,4-DIMETHYL-2,6-DIOXOCYCLOHEXYLIDENE)-3-METHYLBUTYL]AMINO]BENZYL ESTER
CBNumber:
CB9307458
Molecular Formula:
C39H42N2O8
Molecular Weight:
666.76
MOL File:
269066-08-2.mol
MSDS File:
SDS
Modify Date:
2024/7/2 8:55:41

FMOC-ASP(ODMAB)-OH Properties

Boiling point 841.0±65.0 °C(Predicted)
Density 1.264±0.06 g/cm3(Predicted)
storage temp. Inert atmosphere,2-8°C
pka 3.51±0.23(Predicted)
form Solid
color White to yellow

FMOC-ASP(ODMAB)-OH Chemical Properties,Uses,Production

Chemical Properties

Light yellow to off-white powder

Uses

The Dmab group can be cleaved selectively in the presence of tBu-based protected groups by treatment with 2% hydrazine in DMF, making this derivative an extremely useful tool for the preparation of cyclic peptides by FMOC SPPS

FMOC-ASP(ODMAB)-OH Preparation Products And Raw materials

Raw materials

Preparation Products

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FMOC-L-ASPARTIC ACID BETA-4-[N-[1-(4,4-DIMETHYL-2,6-DIOXOCYCLOHEXYLIDENE)-3-METHYLBUTYL]AMINO]BENZYL ESTER FMOC-ASP(ODMAB)-OH FMOC-ASPARTIC ACID(ODMAB) N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-L-ASPARTIC ACID BETA-4-[N-[1-(4,4-DIMETHYL-2,6-DIOXOCYCLOHEXYLIDENE)-3-METHYLBUTYL]AMINO]BENZYL ESTER N-ALPHA-FMOC-L-ASPARTIC ACID BETA-4-[N-[1-(4,4-DIMETHYL-2,6-DIOXOCYCLOHEXYLIDENE)-3-METHYLBUTYL]-AMINO] BENZYL ESTER Fomc-Asp(Odmab)-OH N-[(9H-Fluoren-9-ylmethoxy)carbonyl]-L-aspartic acid 4-[[4-[[1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl]amino]phenyl]methyl] ester (S)-2-(((9H-fluoren-9-yl)methyl9H-fluoren-9-yl)methoxy)carbonylamino)-4-(4-(1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutylamino)benzyloxy)-4-oxobutanoic acid Fmoc-L-aspartic acid beta-4-[N-{1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl}amino]benzyl ester FMoc-L-aspartic acid b-4-[N-{1-(4,4-diMethyl-2,6-dioxocyclohexylidene)-3-Methylbutyl}aMino]benzyl ester (S)-2-((((9H-Fluoren-9-yl)Methoxy)carbonyl)aMino)-4-((4-((1-(4,4-diMethyl-2,6-dioxocyclohexylidene)-3-Methylbutyl)aMino)benzyl)oxy)-4-oxobutanoic acid Fmoc-L-Asp(ODmab)-OH Fmoc-L-aspartic acid β-4-[N-{1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl}amino]benzyl ester≥ 98% (HPLC) (9H-Fluoren-9-yl)MethOxy]Carbonyl Asp(ODMAB)-OH (2S)-4-[(4-{[1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl]amino}phenyl)methoxy]-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-oxobutanoic acid L-Aspartic acid, N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, 4-[[4-[[1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl]amino]phenyl]methyl] ester (2S)-4-[[4-[[1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl]amino]phenyl]methoxy]-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-oxobutanoicaci FMOC-ASP(ODMAB)-OH USP/EP/BP Fmoc-L-aspartic acid β-4-[N-{1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl}amino]benzyl ester 269066-08-2 C39H42N2O8 Fmoc Amino Acids amino acid