64528-94-5 Usage
Uses
Used in Enzyme Research:
1,3-DIBROMOPROPANE-1,1,3,3-D4 is used as a research tool for studying the substrate specificity of haloalkane dehalogenases. It aids in understanding the enzyme's ability to recognize and process halogenated propane molecules, providing insights into the enzyme's structure, function, and potential applications in bioremediation and detoxification processes.
Used in Bioremediation Applications:
In the field of bioremediation, 1,3-DIBROMOPROPANE-1,1,3,3-D4 can be employed to evaluate the effectiveness of haloalkane dehalogenases in breaking down environmental pollutants, such as halogenated hydrocarbons. This can contribute to the development of strategies for cleaning up contaminated sites and reducing the environmental impact of these harmful chemicals.
Used in Pharmaceutical Development:
1,3-DIBROMOPROPANE-1,1,3,3-D4 may also be utilized in the development of new pharmaceuticals targeting haloalkane dehalogenases. By understanding the enzyme's substrate specificity, researchers can design drugs that modulate the enzyme's activity, potentially leading to treatments for various diseases and conditions related to the metabolism of halogenated compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 64528-94-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,5,2 and 8 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 64528-94:
(7*6)+(6*4)+(5*5)+(4*2)+(3*8)+(2*9)+(1*4)=145
145 % 10 = 5
So 64528-94-5 is a valid CAS Registry Number.
64528-94-5Relevant academic research and scientific papers
Conformational dynamic investigation of 1,5-benzodiazepin and its dimethyl derivative by 1H and 13C nmr
Menard, D.,St-Jacques, M.
, p. 1160 - 1168 (2007/10/02)
The conformational and dynamic properties of 1,5-dioxa-6,7-benzocycloheptene (2; 1,5-benzodiazepin) and its dimethyl derivative (7) have been investigated by dinamic 1H and 13C nmr methods.Analysis of the spectra at low temperatures (below coalescence) indicates that the most stable seven-membered ring conformations detected for solutions in CHF2Cl are a mixture of the chair (C, 80percent) and the twist-boat (TB, 20percent) for 2 and a mixture of TB (64percent) and C (36percent) for 7.Free energy barriers were determined for the chair inversion of 2 (6.5 kcal/mol) and 7 (7.5 kcal/mol) as well as for the twist-boat pseudorotation of 7 (6.8 kcal/mol).The conformational properties of these seven-membered heterocycles are discussed and compared to those known for 2,4-benzodiazepins.
