87638-26-4 Usage
General Description
(2R)-2,3-diaminopropan-1-ol is a chemical compound with the molecular formula C3H10N2O. It is a chiral molecule, meaning it has two enantiomers, or mirror-image forms, designated as (2R) and (2S). (2R)-2,3-diaminopropan-1-ol has two amino groups and one hydroxyl group attached to the carbon backbone. (2R)-2,3-diaminopropan-1-ol is commonly used as a chiral building block in organic synthesis and pharmaceutical research, as well as in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. It also has potential applications in the development of chiral catalysts and ligands for asymmetric catalysis.
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.
