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(+/-)-Cbz-alpha-phosphono-D-alanine (CPDA) is a synthetic chemical compound that serves as a building block or intermediate in the synthesis of various pharmaceuticals and biologically active molecules. It is derived from D-alanine, an amino acid, and features a carbobenzoxy (Cbz) protecting group and a phosphonate group at the alpha position. The unique structure and properties of CPDA make it a valuable tool in medicinal chemistry and drug discovery research, with potential therapeutic applications in the development of antiviral and antitumor agents.

83026-99-7

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83026-99-7 Usage

Uses

Used in Pharmaceutical Synthesis:
(+/-)-Cbz-alpha-phosphono-D-alanine is used as a building block for the synthesis of various pharmaceuticals and biologically active molecules. Its unique structure allows for the development of new compounds with potential therapeutic applications.
Used in Antiviral Applications:
(+/-)-Cbz-alpha-phosphono-D-alanine is used as a potential antiviral agent. Its phosphonate group can inhibit viral replication by targeting key enzymes or proteins involved in the viral life cycle, thereby reducing viral load and preventing the spread of infection.
Used in Antitumor Applications:
(+/-)-Cbz-alpha-phosphono-D-alanine is used as a potential antitumor agent. Its unique structure can be utilized to target specific enzymes or pathways involved in tumor growth and progression, leading to the inhibition of cancer cell proliferation and the promotion of cell death.
Used in Medicinal Chemistry Research:
(+/-)-Cbz-alpha-phosphono-D-alanine is used as a valuable tool in medicinal chemistry research. Its properties can be explored to understand the interactions between compounds and biological targets, facilitating the design and optimization of new therapeutic agents.
Used in Drug Discovery:
(+/-)-Cbz-alpha-phosphono-D-alanine is used in drug discovery to identify and develop new pharmaceuticals with improved efficacy and safety profiles. Its unique structure can be modified or combined with other compounds to create novel drug candidates for various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 83026-99-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,2 and 6 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 83026-99:
(7*8)+(6*3)+(5*0)+(4*2)+(3*6)+(2*9)+(1*9)=127
127 % 10 = 7
So 83026-99-7 is a valid CAS Registry Number.

83026-99-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 2-(benzyloxycarbonylamino)-2-dimethoxyphosphoryl-acetate

1.2 Other means of identification

Product number -
Other names 2-Benzyloxycarbonylamino-2-diethyloxyphosphoryl-essigsaeure-ethylester

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:83026-99-7 SDS

83026-99-7Downstream Products

83026-99-7Relevant academic research and scientific papers

N-H insertion reactions of rhodium carbenoids. Part 2. Preparation of N-substituted amino(phosphoryl)acetates (N-substituted phosphorylglycine esters)

Ferris, Leigh,Haigh, David,Moody, Christopher J.

, p. 2885 - 2888 (2007/10/03)

Rhodium(II) acetate-catalysed reaction of ethyl 2-diazo-2-diethoxyphosphorylacetate 2 with carbamates, amides, ureas or anilines gives a range of N-substituted 2-amino-2-diethoxyphosphorylacetates 3-18 by N-H insertion reaction of the intermediate rhodium

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