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FMOC-D-IGL-OH is a chemical compound that features a fluorenylmethyloxycarbonyl (FMOC) protecting group attached to the amino acid sequence D-isoleucine-glycine-leucine (D-IGL), along with a hydroxyl (OH) functional group. FMOC-D-IGL-OH plays a crucial role in peptide synthesis, serving as a building block for creating peptides with specific sequences and structures. The FMOC group shields the amino acid from unwanted reactions during the synthesis process, while the D-IGL segment imparts particular biological and structural characteristics to the peptide. The hydroxyl group enhances the compound's versatility in peptide chemistry by enabling participation in a range of chemical reactions. FMOC-D-IGL-OH is thus a significant component in peptide synthesis, with broad applications in the development of biologically active compounds.

205526-40-5

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205526-40-5 Usage

Uses

Used in Pharmaceutical Industry:
FMOC-D-IGL-OH is used as a building block in peptide synthesis for the development of biologically active compounds. FMOC-D-IGL-OH's specific sequence and structure contribute to the creation of peptides with targeted biological functions, making it valuable for designing drugs with precise therapeutic effects.
Used in Research and Development:
In the field of research, FMOC-D-IGL-OH is utilized as a component in the synthesis of custom peptides for studying their interactions with biological systems. This allows scientists to explore the compound's potential in understanding disease mechanisms, developing diagnostic tools, and creating novel therapeutic agents.
Used in Biochemistry and Molecular Biology:
FMOC-D-IGL-OH serves as a versatile tool in biochemistry and molecular biology for constructing peptides with specific properties. FMOC-D-IGL-OH's ability to be modified and its incorporation into larger peptide structures make it instrumental in studying protein functions, developing vaccines, and engineering new biomaterials.
Used in Peptide Drug Design:
FMOC-D-IGL-OH is employed as a key component in the design of peptide drugs, where its specific sequence and the protective FMOC group allow for the creation of peptides with enhanced stability and bioactivity. This is particularly important in the development of drugs that require precise targeting and minimal side effects.
Overall, FMOC-D-IGL-OH's applications span across various scientific and medical disciplines, highlighting its importance in the synthesis of peptides with diverse and specific functions.

Check Digit Verification of cas no

The CAS Registry Mumber 205526-40-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,5,5,2 and 6 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 205526-40:
(8*2)+(7*0)+(6*5)+(5*5)+(4*2)+(3*6)+(2*4)+(1*0)=105
105 % 10 = 5
So 205526-40-5 is a valid CAS Registry Number.

205526-40-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-(2,3-dihydro-1H-inden-2-yl)-2-(9H-fluoren-9-ylmethoxycarbonylamino)acetic acid

1.2 Other means of identification

Product number -
Other names (R)-2,3-dihydro-1H-inden-2-yl({[(9H-fluoren-9-ylmethoxy)carbonyl]amino})acetic acid

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:205526-40-5 SDS

205526-40-5Upstream product

205526-40-5Downstream Products

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