87638-26-4 Usage
Description
(2R)-2,3-diaminopropan-1-ol is a chiral chemical compound with the molecular formula C3H10N2O. It features two amino groups and one hydroxyl group attached to the carbon backbone, and it exists in two enantiomers, (2R) and (2S), with the (2R) form being the focus of this description.
Uses
Used in Organic Synthesis:
(2R)-2,3-diaminopropan-1-ol is utilized as a chiral building block in organic synthesis, playing a crucial role in the creation of various complex organic molecules.
Used in Pharmaceutical Research:
In pharmaceutical research, (2R)-2,3-diaminopropan-1-ol serves as a key intermediate for the development of new pharmaceuticals, contributing to the advancement of medical treatments.
Used in Production of Pharmaceuticals:
(2R)-2,3-diaminopropan-1-ol is used as a starting material in the production of various pharmaceuticals, highlighting its importance in the healthcare industry.
Used in Agrochemicals:
This chiral compound is also employed in the development and synthesis of agrochemicals, which are essential for agricultural productivity and pest control.
Used in Specialty Chemicals:
(2R)-2,3-diaminopropan-1-ol finds application in the production of specialty chemicals, which are used in specific industries for unique purposes.
Used in Chiral Catalysts and Ligands Development:
(2R)-2,3-diaminopropan-1-ol has potential applications in the development of chiral catalysts and ligands for asymmetric catalysis, a field that is vital for the synthesis of enantiomerically pure compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 87638-26-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,6,3 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 87638-26:
(7*8)+(6*7)+(5*6)+(4*3)+(3*8)+(2*2)+(1*6)=174
174 % 10 = 4
So 87638-26-4 is a valid CAS Registry Number.
87638-26-4Relevant articles and documents
Synthesis and antitumor activity of Pt(II) complexes containing 2,3-diaminopropanol isomers
Noji,Motoama,Tashiro,Kidani
, p. 1469 - 1473 (1983)
Halogeno, sulfato, and nitrato Pt(II) complexes of 2,3-diaminopropranolol (pnOH) isomers were synthesized and their activities against leukemia L1210 were tested. The conformations of their chelate rings were determined to be λ- and δ-gauche forms for R- and S-pnOH, respectively, by 13C-nuclear magnetic resonance and circular dichroism spectral analyses. Among the pnOH isomers, Pt(II) complexes containing R-pnOH showed higher antitumor activity than those containing S- or racemic pnOH. It seems that there may be a relationship between the conformations of the chelate rings and antitumor activity in the case of five-membered chelate rings.
