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N-FMoc-2-amino-2-(3-butenyl)hex-5-enoic acid is a synthetic derivative of the natural amino acid lysine, featuring a Fluorenylmethyloxycarbonyl (FMoc) protecting group and a 2-amino-2-(3-butenyl)hex-5-enoic acid side chain. N-FMoc-2-amino-2-(3-butenyl)hex-5-enoic acid is designed for controlled and selective deprotection during peptide synthesis, offering specific functionalization and reactivity in peptide chemistry. Its unique structure makes it a valuable building block for creating diverse peptide structures, suitable for pharmaceutical, biotechnological, and academic research applications.

1311992-98-9

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1311992-98-9 Usage

Uses

Used in Pharmaceutical Industry:
N-FMoc-2-amino-2-(3-butenyl)hex-5-enoic acid is used as a key building block for the synthesis of bioactive peptides and proteins. Its side chain allows for the incorporation of specific functionalities and reactivity, enabling the development of novel therapeutic agents with tailored properties and improved pharmacological profiles.
Used in Biotechnological Applications:
In the biotechnology sector, N-FMoc-2-amino-2-(3-butenyl)hex-5-enoic acid serves as a versatile component in the engineering of peptides and proteins with desired characteristics. Its unique side chain facilitates the creation of biocatalysts, biosensors, and other biofunctional materials for various biotechnological processes.
Used in Academic Research:
N-FMoc-2-amino-2-(3-butenyl)hex-5-enoic acid is utilized as a research tool in academic settings to explore the fundamental aspects of peptide chemistry and protein engineering. Its controlled deprotection and specific reactivity enable the investigation of novel synthetic strategies, structural motifs, and functional properties of peptides and proteins.

Check Digit Verification of cas no

The CAS Registry Mumber 1311992-98-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,1,9,9 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1311992-98:
(9*1)+(8*3)+(7*1)+(6*1)+(5*9)+(4*9)+(3*2)+(2*9)+(1*8)=159
159 % 10 = 9
So 1311992-98-9 is a valid CAS Registry Number.
InChI:InChI=1S/C25H27NO4/c1-3-5-15-25(23(27)28,16-6-4-2)26-24(29)30-17-22-20-13-9-7-11-18(20)19-12-8-10-14-21(19)22/h3-4,7-14,22H,1-2,5-6,15-17H2,(H,26,29)(H,27,28)

1311992-98-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-but-3-enyl-2-(9H-fluoren-9-ylmethoxycarbonylamino)hex-5-enoic a cid

1.2 Other means of identification

Product number -
Other names -

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:1311992-98-9 SDS

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