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201731-77-3

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201731-77-3 Usage

Description

H-D-ALA-PNA . HCL is a chemical compound consisting of H-D-ALA-PNA, a peptide nucleic acid (PNA) monomer, and hydrochloric acid (HCL). H-D-ALA-PNA is a modified PNA with an N-terminal D-alanine residue, which may enhance its stability and binding properties. PNAs are synthetic molecules that mimic the structure of DNA using a backbone of N-(2-aminoethyl)glycine units linked by peptide bonds. HCL is a strong acid used in chemical processes to adjust pH or facilitate reactions. H-D-ALA-PNA . HCL is a compound used in molecular biology and biochemistry research to study nucleic acids and their interactions with other molecules.

Uses

Used in Molecular Biology Research:
H-D-ALA-PNA . HCL is used as a research tool for studying the structure, function, and interactions of nucleic acids, particularly DNA and RNA. Its modified PNA structure allows for enhanced stability and binding properties, making it a valuable compound for investigating nucleic acid interactions.
Used in Biochemistry Research:
H-D-ALA-PNA . HCL is used as a reagent in biochemistry research to explore the interactions between nucleic acids and other biomolecules, such as proteins and enzymes. Its unique properties may provide insights into the mechanisms of nucleic acid recognition and binding, contributing to the understanding of biological processes.
Used in Drug Development:
H-D-ALA-PNA . HCL may be used as a starting material or intermediate in the development of new drugs targeting nucleic acid-related diseases. Its modified PNA structure and enhanced binding properties could potentially be leveraged to design drugs with improved specificity and efficacy.
Used in Diagnostic Applications:
H-D-ALA-PNA . HCL could be employed in the development of diagnostic tools and assays for detecting and analyzing nucleic acid sequences. Its modified PNA structure may offer advantages in terms of specificity and sensitivity compared to traditional DNA or RNA probes.
Used in Nanotechnology:
H-D-ALA-PNA . HCL may be utilized in the field of nanotechnology for the design and synthesis of nanoscale devices and materials with applications in medicine, electronics, and other industries. Its unique properties and interactions with nucleic acids could contribute to the development of innovative nanostructures with specific functions.

Check Digit Verification of cas no

The CAS Registry Mumber 201731-77-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,7,3 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 201731-77:
(8*2)+(7*0)+(6*1)+(5*7)+(4*3)+(3*1)+(2*7)+(1*7)=93
93 % 10 = 3
So 201731-77-3 is a valid CAS Registry Number.

201731-77-3SDS

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 2-amino-N-(4-nitrophenyl)propanamide,hydrochloride

1.2 Other means of identification

Product number -
Other names D-Alanine 4-nitroanilide hydrochloride

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:201731-77-3 SDS

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