171815-92-2 Usage
Uses
Used in Medicinal Chemistry:
(2R,3S)-1-CHLORO-3-DIBENZYLAMINO-5-METHYLHEXAN-2-OL is used as a chiral molecule in medicinal chemistry for its potential to interact with biological systems in specific ways due to its unique arrangement of atoms and functional groups.
Used in Drug Development:
In the pharmaceutical industry, (2R,3S)-1-CHLORO-3-DIBENZYLAMINO-5-METHYLHEXAN-2-OL is utilized as a compound with potential applications in drug development, given its structural features that may facilitate targeted interactions with biological targets, thus warranting further research into its properties and therapeutic potential.
Further exploration and research are required to fully understand the compound's properties and to determine its suitability for specific applications in medicine and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 171815-92-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,1,8,1 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 171815-92:
(8*1)+(7*7)+(6*1)+(5*8)+(4*1)+(3*5)+(2*9)+(1*2)=142
142 % 10 = 2
So 171815-92-2 is a valid CAS Registry Number.
InChI:InChI=1/C21H28ClNO/c1-17(2)13-20(21(24)14-22)23(15-18-9-5-3-6-10-18)16-19-11-7-4-8-12-19/h3-12,17,20-21,24H,13-16H2,1-2H3/t20-,21-/m0/s1
171815-92-2Relevant academic research and scientific papers
Total selective synthesis of enantiopure O1-acyl-3-aminoalkane- 1,2-diols by ring opening of aminoepoxides with carboxylic acids
Concellon, Jose M.,Suarez, Jose Ramon,Del Solar, Virginia,Llavona, Ricardo
, p. 10348 - 10353 (2007/10/03)
Synthesis of (2R,3S)- or (2S,3S)-O1-acyl-3-aminoalkane-1,2-diols by ring opening of enantiopure (2R,1′S)- or (2S,1′S)-2-(1- aminoalkyl)epoxides 1 or 2, with carboxylic acids in the presence of BF 3·Et2O and chlorotrimethyl
Highly Diastereoselective Synthesis of Threo or Erythro Aminoalkyl Epoxides from α-Amino Acids
Barluenga, Jose,Baragana, Beatriz,Concellon, Jose M.
, p. 6696 - 6699 (2007/10/03)
α-Chloro-α'-(dibenzylamino)methylketones 3 are synthesized in enantiomerically pure form starting from α-amino acids.Reduction of amino ketones 3 and further epoxidation affords threo aminoalkyl epoxides 6 with diastereoisomeric excess ranging between 94percent and 98percent.The synthesis of erythro amino epoxides 9 is also described by reaction of α-amino aldehydes 7 with in situ generated (halomethyl)lithium.Amino epoxides 9 were obtained with a diastereoisomeric excess ranging between 91percent and 98percent.
