136597-79-0 Usage
Description
(2R,3R)-2,3-BIS(BUTYLAMINO)BUTANE-1,4-DIOL is a chiral chemical compound with the molecular formula C12H28N2O2. It possesses two stereoisomers due to its chiral nature. (2R,3R)-2,3-BIS(BUTYLAMINO)BUTANE-1,4-DIOL is primarily utilized as a chiral building block in organic synthesis, particularly for the production of pharmaceuticals and agrochemicals.
Uses
Used in Pharmaceutical Industry:
(2R,3R)-2,3-BIS(BUTYLAMINO)BUTANE-1,4-DIOL is used as a chiral building block for the synthesis of complex molecules and pharmaceuticals. Its unique structure and chiral properties make it a valuable tool in creating enantiomerically pure compounds, which are essential for the development of effective and safe medications.
Used in Agrochemical Industry:
In the agrochemical industry, (2R,3R)-2,3-BIS(BUTYLAMINO)BUTANE-1,4-DIOL serves as a chiral building block for the synthesis of enantiomerically pure agrochemicals. This ensures the development of more targeted and environmentally friendly products.
Used in Chiral Catalysts:
(2R,3R)-2,3-BIS(BUTYLAMINO)BUTANE-1,4-DIOL is used as a chiral catalyst in various chemical reactions. Its chiral properties enable the selective formation of desired enantiomers, improving the efficiency and selectivity of the synthesis process.
Used in Chiral Ligands:
(2R,3R)-2,3-BIS(BUTYLAMINO)BUTANE-1,4-DIOL is also employed as a chiral ligand in asymmetric catalysis. Its unique structure aids in the enantioselective synthesis of complex molecules, which is crucial for the development of advanced pharmaceuticals and agrochemicals.
Used as a Chiral Resolving Agent:
(2R,3R)-2,3-BIS(BUTYLAMINO)BUTANE-1,4-DIOL is utilized as a chiral resolving agent to separate enantiomers. This is important for obtaining pure enantiomers, which is essential for the safety and efficacy of pharmaceuticals and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 136597-79-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,5,9 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 136597-79:
(8*1)+(7*3)+(6*6)+(5*5)+(4*9)+(3*7)+(2*7)+(1*9)=170
170 % 10 = 0
So 136597-79-0 is a valid CAS Registry Number.
136597-79-0Relevant articles and documents
β,γ-Bis-substituted PNA with configurational and conformational switch: Preferred binding to cDNA/RNA and cell-uptake studies
Bose, Tanaya,Banerjee, Anjan,Nahar, Smita,Maiti, Souvik,Kumar, Vaijayanti A.
supporting information, p. 7693 - 7696 (2015/07/27)
(S,S)- and (R,R)-β,γ-Bis-substituted PNAs were synthesized from the C-2 symmetric vicinal diamine system embedded in 1,4 dihydroxybutane and 1,4-dimethoxybutane scaffolds. (R,R)-β,γ-Bis-methoxymethyl-PNA derived from d-tartaric acid was found to be in the
Efficient synthesis of (2R,3R)- and (2S,3S)-2,3-diaminobutane-1,4-diol and their dibenzyl ethers
Scheurer, Andreas,Mosset, Paul,Saalfrank, Rolf W.
, p. 1243 - 1251 (2007/10/03)
(2R,3R)-2,3-Diaminobutane-1,4-diol 6 and its dibenzyl ether 7 were efficiently synthesized starting from L-tartaric acid 1a. The crucial step, debenzylation of intermediate dibenzyloxydiazide 4, was accomplished in good yield by boron trichloride-dimethyl sulfide complex. The enantiomeric series was similarly obtained starting from D-tartaric acid.
Synthesis of chiral 2,3-disubstituted 1,4-diazabicyclo [2.2.2] octane. New ligand for the osmium-catalyzed asymmetric dihydroxylation of olefins
Oishi, Tohru,Hirama, Masahiro
, p. 639 - 642 (2007/10/02)
Chiral 2,3-disubstituted 1,4-diazabicyclo[2.2.2]octane (DABCO) derivatives have been synthesized and utilized as a chiral ligand for the osmium-catalyzed asymmetric dihydroxylation of olefins. Optically active diols in up to 41%ee are obtained in good yields.
