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204260-38-8

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204260-38-8 Usage

General Description

FMOC-D-4-Methylphe, also known as Fmoc-D-(4-Me)Phe-OH, is a chemical compound utilized in the scientific research particularly in the field of biochemistry. This chemical is an Fmoc N-protected amino acid derivative, where Fmoc refers to the fluorenylmethyloxycarbonyl group utilized to protect the amino group in peptide synthesis. The "D" in its name indicates that it is a right-handed isomer, part of a group called D-amino acids. The "4-Methylphe" part refers to the specific amino acid known as phenylalanine which has been modified by adding a methyl group, thereby altering its chemical properties. This type of modified, protected amino acid is typically used in peptide synthesis, a process of creating peptides, which are small proteins, in a lab setting.

Check Digit Verification of cas no

The CAS Registry Mumber 204260-38-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,2,6 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 204260-38:
(8*2)+(7*0)+(6*4)+(5*2)+(4*6)+(3*0)+(2*3)+(1*8)=88
88 % 10 = 8
So 204260-38-8 is a valid CAS Registry Number.

204260-38-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(4-methylphenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names FMOC-P-ME-D-PHE-OH

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:204260-38-8 SDS

204260-38-8Relevant articles and documents

Ligand-Enabled β-C–H Arylation of α-Amino Acids Without Installing Exogenous Directing Groups

Chen, Gang,Zhuang, Zhe,Li, Gen-Cheng,Saint-Denis, Tyler G.,Hsiao, Yi,Joe, Candice L.,Yu, Jin-Quan

, p. 1506 - 1509 (2017/02/05)

Herein we report acid-directed β-C(sp3)-H arylation of α-amino acids enabled by pyridine-type ligands. This reaction does not require the installation of an exogenous directing group, is scalable, and enables the preparation of Fmoc-protected unnatural amino acids in three steps. The pyridine-type ligands are crucial for the development of this new C(sp3)-H arylation.

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