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FMOC-(S)-3-AMINO-3-(3,5-DIMETHOXY-PHENYL)-PROPIONIC ACID is a specialized chemical compound utilized in the field of peptide synthesis and pharmaceutical research. It features a fluorenylmethyloxycarbonyl (FMOC) protecting group that is attached to a chiral amino acid, which includes a 3,5-dimethoxy-phenyl group. FMOC-(S)-3-AMINO-3-(3,5-DIMETHOXY-PHENYL)-PROPIONIC ACID is recognized for its role as a building block in the creation of peptides and other intricate organic molecules, with the FMOC group serving as a temporary protective agent. This allows for selective modification and integration of the amino acid into larger peptide chains. The presence of a chiral center in the amino acid enhances its utility in the production of pharmaceuticals and bioactive molecules with precise stereochemistry.

501015-38-9

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501015-38-9 Usage

Uses

Used in Pharmaceutical Research and Development:
FMOC-(S)-3-AMINO-3-(3,5-DIMETHOXY-PHENYL)-PROPIONIC ACID is used as a key building block for the synthesis of peptides and complex organic molecules, particularly in the development of new pharmaceuticals. Its application is crucial for the creation of stereochemically pure compounds, which are essential for ensuring the desired biological activity and minimizing potential side effects.
Used in Peptide Synthesis:
In the field of peptide synthesis, FMOC-(S)-3-AMINO-3-(3,5-DIMETHOXY-PHENYL)-PROPIONIC ACID is employed as a protected amino acid. The FMOC group allows for selective incorporation of the amino acid into growing peptide chains, facilitating the stepwise assembly of peptides with high precision and yield.
Used in Organic Chemistry:
FMOC-(S)-3-AMINO-3-(3,5-DIMETHOXY-PHENYL)-PROPIONIC ACID is also utilized in organic chemistry for the synthesis of various bioactive molecules. The presence of the 3,5-dimethoxy-phenyl group provides unique structural features that can be exploited in the design and synthesis of novel compounds with potential applications in medicine, agriculture, and other industries.
Used in the Synthesis of Stereochemically Pure Compounds:
FMOC-(S)-3-AMINO-3-(3,5-DIMETHOXY-PHENYL)-PROPIONIC ACID is used as a chiral starting material for the synthesis of enantiomerically pure pharmaceuticals and other biologically active substances. The chiral center in the amino acid ensures that the final product has a specific three-dimensional arrangement, which is critical for the compound's interaction with biological targets and its overall efficacy.

Check Digit Verification of cas no

The CAS Registry Mumber 501015-38-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,0,1 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 501015-38:
(8*5)+(7*0)+(6*1)+(5*0)+(4*1)+(3*5)+(2*3)+(1*8)=79
79 % 10 = 9
So 501015-38-9 is a valid CAS Registry Number.

501015-38-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S)-3-(3,5-dimethoxyphenyl)-3-(9H-fluoren-9-ylmethoxycarbonylamino)propanoic acid

1.2 Other means of identification

Product number -
Other names (3S)-3-(3,5-DIMETHOXYPHENYL)-3-[(FLUOREN-9-YLMETHOXY)CARBONYLAMINO]PROPANOIC A CID

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:501015-38-9 SDS

501015-38-9Upstream product

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