151630-98-7 Usage
Description
(2S,3S)-2,3-Diaminobutane-1,4-diol, also known as DAB, is a chiral diol compound that contains two amino groups. It is commonly used as a chiral building block in organic synthesis and pharmaceutical production. DAB is an important intermediate in the synthesis of chiral drugs and fine chemicals, as it can serve as a starting material for the creation of various chiral molecules. Its chiral nature makes it highly valuable for the development of enantiopure compounds, which are crucial for the pharmaceutical industry and drug development. DAB has also been studied for its potential application in the treatment of neurodegenerative diseases and as a catalyst in certain chemical reactions. Overall, DAB is a versatile and important chemical compound with a variety of potential uses in industry and research.
Uses
Used in Pharmaceutical Industry:
(2S,3S)-2,3-Diaminobutane-1,4-diol is used as a chiral building block for the synthesis of chiral drugs and fine chemicals. Its chiral nature allows for the development of enantiopure compounds, which are essential for the pharmaceutical industry and drug development.
Used in Organic Synthesis:
(2S,3S)-2,3-Diaminobutane-1,4-diol is used as a starting material for the creation of various chiral molecules in organic synthesis, making it a valuable component in the synthesis of complex organic compounds.
Used in Neurodegenerative Disease Treatment:
(2S,3S)-2,3-Diaminobutane-1,4-diol has been studied for its potential application in the treatment of neurodegenerative diseases, offering a promising avenue for therapeutic intervention in conditions such as Alzheimer's and Parkinson's diseases.
Used as a Catalyst in Chemical Reactions:
(2S,3S)-2,3-Diaminobutane-1,4-diol has been explored as a catalyst in certain chemical reactions, demonstrating its versatility and utility in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 151630-98-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,6,3 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 151630-98:
(8*1)+(7*5)+(6*1)+(5*6)+(4*3)+(3*0)+(2*9)+(1*8)=117
117 % 10 = 7
So 151630-98-7 is a valid CAS Registry Number.
151630-98-7Relevant articles and documents
Multiple-Hydrogen-Bond Approach to Uncommon Pd(III) Oxidation State: A Pd-Br Chain with High Conductivity and Thermal Stability
Mian, Mohammad Rasel,Iguchi, Hiroaki,Takaishi, Shinya,Murasugi, Hideaki,Miyamoto, Tatsuya,Okamoto, Hiroshi,Tanaka, Hisaaki,Kuroda, Shin-Ichi,Breedlove, Brian K.,Yamashita, Masahiro
, p. 6562 - 6565 (2017)
A Br-bridged Pd chain complex with the Pd ion in an uncommon +3 oxidation state, [Pd(dabdOH)2Br]Br2 (3), was prepared using a new method involving multiple hydrogen bonds. The PdBr chain complex exhibited superior electrical conductivity and thermal stability. An in-plane ligand with an additional hydrogen donor group (hydroxy group), (2S,3S)-2,3-diaminobutane-1,4-diol (dabdOH), was used to create a multiple-hydrogen-bond network, which effectively shrinks the Pd-Br-Pd distance, stabilizing the Pd(III) state up to its decomposition temperature (443 K). 3 shows semiconducting behavior with quite high electrical conductivity (3-38 S cm-1 at room temperature), which is 106 times larger than the previous record for analogous PdBr chains. Indeed, 3 is the most conductive MX-type chain complex reported so far. The precise positional control of ions via a multiple-hydrogen-bond network is a useful method for controlling the electronic states, thermal stability and conductivity of linear coordination polymers.
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.
