87638-26-4 Usage
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.
