Fmoc-L-His(Boc)-OH Dcha is a chemical compound derived from the amino acid histidine, which is integral to protein structure and function. It is equipped with the Fmoc group at the N-terminus and the Boc group at the side chain, providing protection during synthesis. The inclusion of Dcha as a coupling reagent enhances its utility in peptide and protein chemistry, making Fmoc-L-His(Boc)-OH Dcha an essential component in the synthesis of bioactive peptides and peptidomimetics for applications in medicine and biotechnology.
210820-99-8
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Basic information
- Product Name: FMOC-L-HIS(BOC)-OH DCHA
- Synonyms: N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-IM-(T-BUTYLOXYCARBONYL)-L-HISTIDINE DICYCLOHEXYLAMINE;N-ALPHA-(9-FLUORENYLMETHYLOXYCARBONYL)-N-IM-(TERT-BUTYLOXYCARBONYL)-L-HISTIDINE DICYCLOHEXYLAMINE;FMOC-HIS(BOC)-OH DCHA;FMOC-L-HIS(BOC)-OH DCHA;N(ALPHA)-FMOC-N(IM)-BOC-L-HISTIDINE;N-alpha-(9-Fluorenylmethyloxycarbonyl)-N-im-(t-butyloxycarbonyl)-L-histidinecyclohexylamine;fmoc-his(boc)-oh cyclohexylamine salt;nα-fmoc-n(im)-boc-l-histidine cyclohexylamine salt
- CAS NO:210820-99-8
- Molecular Formula: C26H27N3O6.C6H13N
- Molecular Weight: 576.69
- EINECS: N/A
- Product Categories: N/A
- Mol File: 210820-99-8.mol
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Chemical Properties
- Melting Point: N/A
- Boiling Point: 766.1 °C at 760 mmHg
- Flash Point: 417.1 °C
- Appearance: /
- Density: N/A
- Refractive Index: N/A
- Storage Temp.: −20°C
- Solubility: N/A
- CAS DataBase Reference: FMOC-L-HIS(BOC)-OH DCHA(CAS DataBase Reference)
- NIST Chemistry Reference: FMOC-L-HIS(BOC)-OH DCHA(210820-99-8)
- EPA Substance Registry System: FMOC-L-HIS(BOC)-OH DCHA(210820-99-8)
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Safety Data
- Hazard Codes: N/A
- Statements: N/A
- Safety Statements: 22-24/25
- WGK Germany: 3
- RTECS:
- F: 10
- HazardClass: N/A
- PackingGroup: N/A
- Hazardous Substances Data: 210820-99-8(Hazardous Substances Data)
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210820-99-8 Usage
Uses
Used in Pharmaceutical Industry:Fmoc-L-His(Boc)-OH Dcha is used as a building block for the synthesis of bioactive peptides and peptidomimetics, which are crucial for developing new drugs and therapies. Its role in creating complex peptide structures allows for the exploration of novel treatments and interventions in various medical conditions.
Used in Biotechnology Industry:
Fmoc-L-His(Boc)-OH Dcha is utilized as a component in the development of diagnostic tools and therapeutic agents. Its ability to form stable and functional peptides contributes to the advancement of biotechnological applications, such as biosensors and drug delivery systems.
Used in Research and Development:
Fmoc-L-His(Boc)-OH Dcha is employed as a research tool for studying peptide synthesis and protein engineering. Its protected structure facilitates the exploration of new methods and techniques in peptide chemistry, leading to a better understanding of protein function and the development of innovative bioactive compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 210820-99-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,8,2 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.Calculate Digit Verification of CAS Registry Number 210820-99:
(8*2)+(7*1)+(6*0)+(5*8)+(4*2)+(3*0)+(2*9)+(1*9)=98
98 % 10 = 8
So 210820-99-8 is a valid CAS Registry Number.
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FMOC-L-HIS(BOC)-OH DCHA
