Basic information

Product Name: FMOC-L-SELENOMETHIONINE
Synonyms: N-ALPHA-FMOC-L-SELENOMETHIONINE;FMOC-SEMET-OH;FMOC-L-SELENOMETHIONINE;(S)-2-((((9H-fluoren-9-yl)Methoxy)carbonyl)aMino)-4-(Methylselanyl)butanoic acid;(2S)-2-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-4-(methylseleno)butanoic acid;(9H-Fluoren-9-yl)MethOxy]Carbonyl L-Selenomethionine
CAS NO:1217852-49-7
Molecular Formula: C20H21NO4Se
Molecular Weight: 418.35
EINECS: N/A
Product Categories: Seleno Amino Acid;amino acids
Mol File: 1217852-49-7.mol

Chemical Properties

Melting Point: N/A
Boiling Point: 623.5±55.0 °C(Predicted)
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: 2-8°C
Solubility: N/A
PKA: 3.80±0.10(Predicted)
CAS DataBase Reference: FMOC-L-SELENOMETHIONINE(CAS DataBase Reference)
NIST Chemistry Reference: FMOC-L-SELENOMETHIONINE(1217852-49-7)
EPA Substance Registry System: FMOC-L-SELENOMETHIONINE(1217852-49-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: IRRITANT
PackingGroup: N/A
Hazardous Substances Data: 1217852-49-7(Hazardous Substances Data)

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SDS
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1217852-49-7 Usage

Uses

Used in Peptide and Protein Synthesis:
FMOC-L-Selenomethionine is used as a building block in the synthesis of complex peptide and protein systems. Its incorporation allows for the development of novel bioactive molecules with enhanced properties, such as improved stability, bioavailability, and therapeutic potential.
Used in Backbone Engineering:
FMOC-L-Selenomethionine is used as a key component in the backbone engineering of complex peptide and protein systems. Its unique selenium-containing structure enables the formation of novel conformations and secondary structures, which can lead to the discovery of new bioactive peptides and proteins with specific functions and applications.
Used in the Incorporation of Freidinger Lactams:
FMOC-L-Selenomethionine is used in the incorporation of Freidinger lactams in backbone engineering of complex peptide and protein systems. Freidinger lactams are cyclic structures that can be incorporated into peptides to induce specific conformations and improve their stability. The combination of FMOC-L-Selenomethionine and Freidinger lactams allows for the design of peptides with tailored properties and enhanced biological activities.

Check Digit Verification of cas no

The CAS Registry Mumber 1217852-49-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,8,5 and 2 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1217852-49:
(9*1)+(8*2)+(7*1)+(6*7)+(5*8)+(4*5)+(3*2)+(2*4)+(1*9)=157
157 % 10 = 7
So 1217852-49-7 is a valid CAS Registry Number.

1217852-49-7SDS

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)-4-methylselanyl-buta noic acid

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:1217852-49-7 SDS

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