1421-04-1 Usage
Uses
Used in Pharmaceutical Research:
DL-2,4-Diaminoglutaric acid is used as a research compound for its potential role in the treatment of neurodegenerative disorders such as amyotrophic lateral sclerosis (ALS). Its study is crucial for understanding its therapeutic effects and mechanisms of action in these conditions.
Used in Organic Synthesis:
In the field of organic synthesis, DL-2,4-Diaminoglutaric acid serves as a valuable intermediate or building block for the development of new organic compounds and pharmaceuticals. Its unique structure allows for various chemical reactions that can lead to the creation of novel molecules with potential applications in medicine and other industries.
While the provided materials do not specify different applications across various industries, the general uses outlined above encompass the primary areas where DL-2,4-Diaminoglutaric acid is currently being explored. As research progresses, additional applications may be discovered, further expanding the utility of this compound.
Check Digit Verification of cas no
The CAS Registry Mumber 1421-04-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,4,2 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1421-04:
(6*1)+(5*4)+(4*2)+(3*1)+(2*0)+(1*4)=41
41 % 10 = 1
So 1421-04-1 is a valid CAS Registry Number.
InChI:InChI=1/C5H10N2O4/c6-2(4(8)9)1-3(7)5(10)11/h2-3H,1,6-7H2,(H,8,9)(H,10,11)
1421-04-1Relevant articles and documents
Synthesis of stereoisomers of 2,4-diaminoglutaric and 2,5-diaminoadipic acids
Krasnov, V. P.,Zhdanova, E. A.,Korolyova, M. A.,Bukrina, I. M.,Kodess, M. I.,et al.
, p. 319 - 323 (1997)
Stereoisomers of 2,4-diaminoglutaric and 2,5-diaminoadipic acids were synthesized from glutamic and 2-aminoadipic acids, respectively.The stereochemistry of the products was established by 1H NMR spectroscopy and X-ray analysis. - Keywords: 2,4-diaminoglutaric acid; 2,5-diaminoadipic acid; nucleophilic substitution; stereoisomers; racemization