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FMOC-(S)-3-AMINO-3-(4-METHYL-PHENYL)-PROPIONIC ACID is a chemical compound derived from the amino acid alanine, featuring a 4-methyl-phenyl group and an FMOC (9-fluorenylmethoxycarbonyl) protecting group. FMOC-(S)-3-AMINO-3-(4-METHYL-PHENYL)-PROPIONIC ACID plays a significant role in peptide synthesis and pharmaceutical research, particularly as a chiral auxiliary in asymmetric synthesis, enabling selective modifications and functionalizations in organic chemistry and drug discovery.

479064-99-8

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479064-99-8 Usage

Uses

Used in Pharmaceutical Research:
FMOC-(S)-3-AMINO-3-(4-METHYL-PHENYL)-PROPIONIC ACID is used as a chiral auxiliary for the asymmetric synthesis of various compounds, facilitating the creation of enantiomerically pure products which are crucial in the development of pharmaceuticals with targeted biological activity.
Used in Peptide Synthesis:
In the field of peptide synthesis, FMOC-(S)-3-AMINO-3-(4-METHYL-PHENYL)-PROPIONIC ACID is used as a building block for the construction of peptide sequences. The FMOC group serves as a protecting group for amines, preventing unwanted side reactions during the synthesis process and ensuring the correct formation of peptide bonds.
Used in Organic Chemistry:
FMOC-(S)-3-AMINO-3-(4-METHYL-PHENYL)-PROPIONIC ACID is utilized as a versatile intermediate in organic chemistry for the synthesis of complex organic molecules. The presence of the 4-methyl-phenyl group allows for selective functionalization, making it a valuable tool for the development of novel chemical entities with potential applications in various industries.
Used in Drug Discovery:
FMOC-(S)-3-AMINO-3-(4-METHYL-PHENYL)-PROPIONIC ACID is employed as a key component in the discovery of new drugs. Its unique structural features and the ability to undergo selective modifications make it an attractive candidate for the design and synthesis of bioactive molecules with potential therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 479064-99-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,9,0,6 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 479064-99:
(8*4)+(7*7)+(6*9)+(5*0)+(4*6)+(3*4)+(2*9)+(1*9)=198
198 % 10 = 8
So 479064-99-8 is a valid CAS Registry Number.
InChI:InChI=1/C25H23NO4/c1-16-10-12-17(13-11-16)23(14-24(27)28)26-25(29)30-15-22-20-8-4-2-6-18(20)19-7-3-5-9-21(19)22/h2-13,22-23H,14-15H2,1H3,(H,26,29)(H,27,28)/t23-/m0/s1

479064-99-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names (S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(p-tolyl)propanoic 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:479064-99-8 SDS

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