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FMOC-(S)-3-AMINO-4-(1-NAPHTHYL)-BUTYRIC ACID is a synthetic amino acid that is widely utilized in biochemistry research, especially in peptide synthesis. FMOC-(S)-3-AMINO-4-(1-NAPHTHYL)-BUTYRIC ACID features an FMOC (9-fluorenylmethoxycarbonyl) group that protects the amino end, enabling chemical modifications at the other end of the molecule. The naphthyl group attached to the structure provides additional points for structural modification, making it a valuable resource in the development of novel peptide sequences. Its applications span across various fields, including protein chemistry, enzymology, and pharmacology, where it plays a critical role in the creation of new pharmaceutical compounds and the understanding of biological processes.

270063-38-2

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270063-38-2 Usage

Uses

Used in Biochemistry Research:
FMOC-(S)-3-AMINO-4-(1-NAPHTHYL)-BUTYRIC ACID is used as a synthetic amino acid for the development of novel peptide sequences. Its FMOC protection and naphthyl group attachment facilitate chemical modifications, making it an essential component in peptide synthesis.
Used in Pharmaceutical Compound Development:
FMOC-(S)-3-AMINO-4-(1-NAPHTHYL)-BUTYRIC ACID is used as a key building block in the creation of new pharmaceutical compounds. Its structural versatility allows for the design of innovative drug molecules with potential therapeutic applications.
Used in Protein Chemistry Studies:
FMOC-(S)-3-AMINO-4-(1-NAPHTHYL)-BUTYRIC ACID is used as a research tool in protein chemistry, where it aids in understanding the structure and function of proteins by enabling the synthesis of modified peptide sequences.
Used in Enzymology Research:
FMOC-(S)-3-AMINO-4-(1-NAPHTHYL)-BUTYRIC ACID is used as a component in enzymology studies, where it helps in the investigation of enzyme mechanisms and the development of enzyme inhibitors or activators.
Used in Pharmacology:
FMOC-(S)-3-AMINO-4-(1-NAPHTHYL)-BUTYRIC ACID is used in pharmacological research to develop and study the effects of new drug candidates, as well as to understand the interactions between drugs and biological targets.

Check Digit Verification of cas no

The CAS Registry Mumber 270063-38-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,0,0,6 and 3 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 270063-38:
(8*2)+(7*7)+(6*0)+(5*0)+(4*6)+(3*3)+(2*3)+(1*8)=112
112 % 10 = 2
So 270063-38-2 is a valid CAS Registry Number.
InChI:InChI=1/C29H25NO4/c30-26(16-27(31)32)28(24-15-7-9-18-8-1-2-10-19(18)24)29(33)34-17-25-22-13-5-3-11-20(22)21-12-4-6-14-23(21)25/h1-15,25-26,28H,16-17,30H2,(H,31,32)/t26-,28?/m0/s1

270063-38-2SDS

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 FMOC-(S)-3-AMINO-4-(1-NAPHTHYL)-BUTYRIC ACID

1.2 Other means of identification

Product number -
Other names FMOC-ALA(1-NAPH)-(C*CH2)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:270063-38-2 SDS

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