171815-92-2 Usage
General Description
The chemical compound (2R,3S)-1-chloro-3-dibenzylamino-5-methylhexan-2-ol is a chiral molecule with a specific arrangement of atoms. It is composed of a hexane backbone with a chlorine atom attached to the first carbon, a methyl group connected to the fifth carbon, and a dibenzylamino group linked to the third carbon. The molecule also contains a hydroxyl group, denoted by the "ol" suffix, attached to the second carbon. (2R,3S)-1-CHLORO-3-DIBENZYLAMINO-5-METHYLHEXAN-2-OL may have potential applications in medicinal chemistry and drug development due to its unique structure and functional groups, which could potentially interact with biological systems in specific ways. Further research and exploration of its properties are necessary to fully understand its potential uses.
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 articles and documents
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