57884-47-6 Usage
Description
(1Z)-2,3,4,5-tetrahydroxypentanal oxime (non-preferred name) is a pentanal derivative with the molecular formula C5H11NO4. It features an oxime functional group (R2C=NOH) and four hydroxyl groups attached to the carbon chain. (1Z)-2,3,4,5-tetrahydroxypentanal oxime (non-preferred name) is known for its potential applications in various industries, particularly due to its unique structure and properties.
Uses
Used in Organic Synthesis:
(1Z)-2,3,4,5-tetrahydroxypentanal oxime (non-preferred name) is used as a key intermediate in organic synthesis for the production of various complex organic compounds. Its oxime and hydroxyl groups provide versatile sites for chemical reactions, enabling the synthesis of a wide range of molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (1Z)-2,3,4,5-tetrahydroxypentanal oxime (non-preferred name) is utilized as a building block for the development of new drugs. Its unique structure allows for the creation of molecules with specific biological activities, making it a valuable asset in drug discovery and design.
Used in Chemical Industry:
(1Z)-2,3,4,5-tetrahydroxypentanal oxime (non-preferred name) also finds applications in the chemical industry, where it can be employed as a reagent or catalyst in various chemical processes. Its functional groups can participate in a range of reactions, contributing to the synthesis of different chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 57884-47-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,8,8 and 4 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 57884-47:
(7*5)+(6*7)+(5*8)+(4*8)+(3*4)+(2*4)+(1*7)=176
176 % 10 = 6
So 57884-47-6 is a valid CAS Registry Number.
57884-47-6Relevant articles and documents
ALCOHOL-, DIOL-, AND CARBOHYDRATE-SUBSTITUTED INDENOISOQUINOLINES AS TOPOISOMERASE I INHIBITORS
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Page/Page column 44, (2012/12/13)
The invention described herein pertains to substituted indenoisoquinoline compounds as described herein, wherein RA, RD, W, X and Y are defined herein, pharmaceutical compositions and formulations comprising the indenoisoquinoline compounds, their synthesis, and methods for their use in the treatment and/or prevention of cancer.
AN N.M.R. INVESTIGATION OF THE ALDOPENTOSE OXIMES
Snyder, Joseph R.
, p. 1 - 13 (2007/10/02)
The solution behavior of the aldopentose oximes 1-4 (arabino, lyxo, ribo, and xylo) has been studied by 1H (400 MHz) and 13C (100 MHz) n.m.r. spectroscopy. 1H and 13C chemical-shift assignments have been made for the acyclic E and Z forms of each configurational isomer in 2H2O.The 13C chemical shift assignments have been made primarily through the use of (1-13C)-enriched compounds and 2D 13C-1H shift-correlation spectroscopy.Analysis of the 1H-1H spin-coupling constants indicates that the arabinose and lyxose oximes adopt an extended zig-zag conformation, whereas the ribose and xylose oximes adopt a bent or sickle conformation.
Preparation of aldononitrile acetates using N-methylimidazole as catalyst and solvent
McGinnis, Gary D.
, p. 284 - 292 (2007/10/02)
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