Basic information

Product Name: FMOC-DPR(BOC-AOA)-OH
Synonyms: FMOC-DAP[AC(-O-NHBOC)]-OH;FMOC-DAP(BOC-AOA)-OH;FMOC-DPR(BOC-AOA)-OH;FMOC-L-DAP(BOC-AOA);FMOC-L-DAP(BOC-AOA)-OH;FMOC-L-DAPA(BOC-AOA)-OH;N-ALPHA-(9-FLUORENYLMETHOXYCARBONYL)-N-BETA-(T-BUTOXYCARBONYL-AMINOOXYACETYL)-L-2,3-DIAMINOPROPIONIC ACID;N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-BETA-(TERT-BUTYLOXYCARBONYL-AMINOOXY-ACETYL)-L-2,3-DIAMINOPROPIONIC ACID
CAS NO:600153-12-6
Molecular Formula: C25H29N3O8
Molecular Weight: 499.51
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: 1.304±0.06 g/cm3(Predicted)
Refractive Index: N/A
Storage Temp.: Store at RT.
Solubility: N/A
PKA: 3.41±0.10(Predicted)
CAS DataBase Reference: FMOC-DPR(BOC-AOA)-OH(CAS DataBase Reference)
NIST Chemistry Reference: FMOC-DPR(BOC-AOA)-OH(600153-12-6)
EPA Substance Registry System: FMOC-DPR(BOC-AOA)-OH(600153-12-6)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 600153-12-6(Hazardous Substances Data)

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SDS
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600153-12-6 Usage

Uses

Used in Pharmaceutical Industry:
FMOC-DPR(BOC-AOA)-OH is used as a peptide synthesis reagent for the chemoselective ligation of unprotected peptides. Its ability to introduce a hydroxylamine functionality that couples with aldehyde groups in another peptide unit allows for the efficient and specific formation of peptide bonds, which is crucial in the development of new drugs and therapeutic agents.
Used in Research and Development:
In the field of research and development, FMOC-DPR(BOC-AOA)-OH is used as a key component in the synthesis of various peptide-based compounds. Its chemoselective ligation properties enable researchers to create complex peptide structures with precision, facilitating the study of peptide interactions and the development of novel bioactive molecules.
Used in Chemical Synthesis:
FMOC-DPR(BOC-AOA)-OH is also utilized in chemical synthesis as a versatile building block for the creation of various peptide-based compounds. Its unique properties allow for the formation of stable peptide bonds under mild conditions, making it an attractive option for the synthesis of peptides and other biomolecules with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 600153-12-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,0,1,5 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 600153-12:
(8*6)+(7*0)+(6*0)+(5*1)+(4*5)+(3*3)+(2*1)+(1*2)=86
86 % 10 = 6
So 600153-12-6 is a valid CAS Registry Number.

600153-12-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name	(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[[2-[(2-methylpropan-2-yl)oxycarbonylamino]oxyacetyl]amino]propanoic acid

1.2 Other means of identification

Product number	-
Other names	AmbotzFAA1461

1.3 Recommended use of the chemical and restrictions on use

Identified uses	For industry use only.
Uses advised against	no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number	-
Service hours	Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:600153-12-6 SDS

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