570414-07-2 Usage
Uses
Used in Organic Synthesis:
(2R,3R,4S,5R)-1,2:4,5-Di-O-isopropylidene-3-nonadecanol is used as a chiral building block for the synthesis of complex organic molecules. Its unique stereochemistry and structural features make it a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (2R,3R,4S,5R)-1,2:4,5-Di-O-isopropylidene-3-nonadecanol is used as a key intermediate in the synthesis of chiral drugs. Its specific stereochemistry allows for the selective formation of desired enantiomers, which is crucial for the development of effective and safe medications.
Used in Chiral Pool Synthesis:
(2R,3R,4S,5R)-1,2:4,5-Di-O-isopropylidene-3-nonadecanol is also used in chiral pool synthesis, a strategy that involves the use of chiral compounds as starting materials for the preparation of other chiral compounds. This approach is particularly useful for the synthesis of complex natural products and biologically active molecules.
Used in Analytical Chemistry:
In analytical chemistry, (2R,3R,4S,5R)-1,2:4,5-Di-O-isopropylidene-3-nonadecanol can be employed as a chiral derivatizing agent for the enantioselective analysis of chiral compounds. Its ability to selectively react with specific enantiomers can help in the determination of enantiomeric purity and the study of stereoselective processes.
Check Digit Verification of cas no
The CAS Registry Mumber 570414-07-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,7,0,4,1 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 570414-07:
(8*5)+(7*7)+(6*0)+(5*4)+(4*1)+(3*4)+(2*0)+(1*7)=132
132 % 10 = 2
So 570414-07-2 is a valid CAS Registry Number.
InChI:InChI=1/C25H48O5/c1-6-7-8-9-10-11-12-13-14-15-16-17-18-20-23(30-25(4,5)28-20)22(26)21-19-27-24(2,3)29-21/h20-23,26H,6-19H2,1-5H3/t20-,21-,22-,23?/m1/s1
570414-07-2Relevant academic research and scientific papers
A facile synthesis of phytosphingosine from diisopropylidene-D-mannofuranose
Chiu, Hsin-Yi,Tzou, Der-Lii M.,Patkar, Laxmikant Narhari,Lin, Chun-Cheng
, p. 5788 - 5791 (2007/10/03)
In the present study, an efficient method with a high overall yield for preparing phytosphingosine and an analogue was developed. Starting with commercially available 2,3;5,6-di-O-isopropylidene-D-mannofuranose, a variety of lipid moieties were incorporated to obtain phytosphingosine and an analogue. Through an eight-step manipulation, phytosphingosine was obtained with an overall yield of 57%.
