3381-02-0 Usage
Uses
Used in Research and Development:
(3-PHENYL-PROPYL)-HYDRAZINE is used as a chemical intermediate for [application reason] in the research and development industry. Its unique structure allows for further modification and synthesis of more complex molecules, contributing to the advancement of various chemical and pharmaceutical applications.
Used in Pharmaceutical Industry:
(3-PHENYL-PROPYL)-HYDRAZINE is used as a building block for [application reason] in the pharmaceutical industry. Its potential role in the synthesis of new drugs and active pharmaceutical ingredients makes it a valuable compound for drug discovery and development.
Used in Agrochemical Industry:
(3-PHENYL-PROPYL)-HYDRAZINE is used as a precursor for [application reason] in the agrochemical industry. Its ability to be incorporated into various agrochemical products, such as pesticides and herbicides, highlights its importance in the development of new and effective agricultural solutions.
Check Digit Verification of cas no
The CAS Registry Mumber 3381-02-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,8 and 1 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3381-02:
(6*3)+(5*3)+(4*8)+(3*1)+(2*0)+(1*2)=70
70 % 10 = 0
So 3381-02-0 is a valid CAS Registry Number.
3381-02-0Relevant articles and documents
Temporary inactivation of plasma amine oxidase by alkylhydrazines. A combined enzyme/model study implicates cofactor reduction/reoxidation but cofactor deoxygenation and subsequent reoxygenation in the case of hydrazine itself
Lee,Jeon,Huang,Sayre
, p. 1925 - 1937 (2007/10/03)
It has been known for some time that hydrazine and its methyl and 1,1-dimethyl analogues induce inactivation of the copper-containing quinone-dependent plasma amine oxidase but that the activity recovers over time, suggesting metabolism of all three inhib
Reactions of N-Aminophthalimide With Electrophiles. II. Preparation and Properties of Araldehyde Hydrazones
Hearn, Michael J.,Lucero, Elena R.
, p. 1537 - 1539 (2007/10/02)
N-Aminophthalimide (I) reacted with a variety of aromatic aldehydes to give the related arylideneaminophthalimides (III-X), although typical ketones such as acetone and benzophenone did not under the specific conditions employed.Catalytic reduction of benzylideneaminophthalimide (III) led to N-benzylaminophthalimide (XI), a stable acid-free precursor of benzylhydrazine.
