138374-00-2 Usage
Uses
Used in Pharmaceutical Industry:
2-N-boc-butane-1,2-diamine-hcl is used as a building block for the synthesis of various pharmaceuticals and biologically active molecules. Its Boc protecting group allows for selective reactions on the nitrogen atom, enabling the synthesis of complex molecules with specific functional groups.
Used in Organic Chemistry:
2-N-boc-butane-1,2-diamine-hcl is used as a versatile intermediate in organic synthesis. Its butane backbone and Boc protecting group provide a stable and easily modifiable structure for the development of new organic compounds.
Used in Drug Delivery Systems:
2-N-boc-butane-1,2-diamine-hcl can be used in the development of drug delivery systems, where its water-soluble nature and chemical stability make it suitable for encapsulation and controlled release of active pharmaceutical ingredients.
Used in Chemical Synthesis:
2-N-boc-butane-1,2-diamine-hcl is used as a reagent in various chemical reactions, such as amide formation, peptide synthesis, and the preparation of other nitrogen-containing compounds. Its Boc protecting group allows for selective deprotection and subsequent reactions, enabling the synthesis of diverse chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 138374-00-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,3,7 and 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 138374-00:
(8*1)+(7*3)+(6*8)+(5*3)+(4*7)+(3*4)+(2*0)+(1*0)=132
132 % 10 = 2
So 138374-00-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H20N2O2.ClH/c1-5-7(6-10)11-8(12)13-9(2,3)4;/h7H,5-6,10H2,1-4H3,(H,11,12);1H
138374-00-2Relevant academic research and scientific papers
SYNTHESIS OF 1,2-AMINOAZIDES. CONVERSION TO UNSYMMETRICAL VICINAL DIAMINES BY CATALYTIC HYDROGENATION OR REDUCTIVE ALKYLATION WITH DICHLOROBORANES.
Benalil, Aziza,Carboni, Bertrand,Vaultier, Michel
, p. 8177 - 8194 (2007/10/02)
1,2-aminoazides are easily prepared from 1,2-amino alcohols.Catalytic hydrogenation in the presence of palladium on charcoal or reductive alkylation with dichloroboranes afford with good yields unsymmetrically substituted vicinal diamines.
