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BOC-D-3-NITROPHENYLALANINE is a chemical compound with the molecular formula C16H20N2O6, derived from the amino acid phenylalanine. It features a tert-butoxycarbonyl (BOC) protecting group and a 3-nitrophenyl group, which can be selectively deprotected under specific conditions. BOC-D-3-NITROPHENYLALANINE is a valuable tool in biochemistry and medicinal chemistry for the synthesis of custom peptides and research into protein structure and function.

158741-21-0

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158741-21-0 Usage

Uses

Used in Peptide Synthesis:
BOC-D-3-NITROPHENYLALANINE is used as a building block in the synthesis of peptides and proteins. The BOC protecting group allows for the stepwise addition of amino acids without premature side reactions, while the 3-nitrophenyl group can be selectively deprotected to facilitate the formation of specific peptide sequences.
Used in Biochemistry Research:
In the field of biochemistry, BOC-D-3-NITROPHENYLALANINE is used as a research tool for studying protein structure and function. Its unique properties enable the creation of custom peptides with specific sequences, allowing researchers to investigate the roles and interactions of various proteins in biological systems.
Used in Medicinal Chemistry:
BOC-D-3-NITROPHENYLALANINE is employed in medicinal chemistry for the development of therapeutic peptides and proteins. Its ability to be selectively deprotected and incorporated into peptide chains makes it a useful component in the design and synthesis of bioactive molecules with potential applications in drug discovery and development.
Used in Drug Delivery Systems:
In drug delivery systems, BOC-D-3-NITROPHENYLALANINE can be used as a component in the design of peptide-based drug carriers. Its selective deprotection and incorporation into peptide sequences can enable the development of targeted drug delivery systems, improving the bioavailability and therapeutic efficacy of various pharmaceutical agents.
Used in Chemical Synthesis Industry:
BOC-D-3-NITROPHENYLALANINE is used as a key intermediate in the synthesis of various chemical compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure and reactivity make it a valuable building block for the development of novel and innovative chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 158741-21-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,7,4 and 1 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 158741-21:
(8*1)+(7*5)+(6*8)+(5*7)+(4*4)+(3*1)+(2*2)+(1*1)=150
150 % 10 = 0
So 158741-21-0 is a valid CAS Registry Number.

158741-21-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-(3-nitrophenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names Boc-L-phe(3-NO2)-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:158741-21-0 SDS

158741-21-0Relevant academic research and scientific papers

Gonadotropin-Releasing Hormone Antagonists: Novel Members of the Azaline B Family

Rivier, Jean E.,Jiang, Guangcheng,Porter, John,Hoeger, Carl A.,Craig, A. Grey,et al.

, p. 2649 - 2662 (2007/10/03)

A series of antagonists of gonadotropin-releasing hormone (GnRH) homologous to azaline B (1, DCpa2, DPal3, Aph5(Atz), DAph6(Atz), ILys8, DAla10>GnRH) was synthesized, cha

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