1743-07-3 Usage
Description
(1,2,3,4-tetrahydronaphthalen-2-yl)hydrazine is an organic compound with the molecular formula C10H16N2. It belongs to the hydrazine class of chemicals and is a derivative of tetrahydronaphthalene, a bicyclic hydrocarbon. (1,2,3,4-tetrahydronaphthalen-2-yl)hydrazine has potential applications in organic synthesis and chemical research, although its specific uses and properties have not been extensively reported in the scientific literature.
Uses
Used in Organic Synthesis:
(1,2,3,4-tetrahydronaphthalen-2-yl)hydrazine is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure allows it to be a versatile building block in the synthesis of complex molecules.
Used in Chemical Research:
(1,2,3,4-tetrahydronaphthalen-2-yl)hydrazine serves as a subject of study in chemical research, where its properties and reactivity can be explored. This can lead to a better understanding of its potential applications and the development of new synthetic methods or chemical reactions involving this compound.
Note: Since the provided materials do not specify particular industries or detailed applications, the uses listed above are general and based on the compound's classification and potential in organic synthesis and chemical research.
Check Digit Verification of cas no
The CAS Registry Mumber 1743-07-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,4 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1743-07:
(6*1)+(5*7)+(4*4)+(3*3)+(2*0)+(1*7)=73
73 % 10 = 3
So 1743-07-3 is a valid CAS Registry Number.
1743-07-3Relevant articles and documents
Efficient Methodology for the Preparation of β-Aminotetralin Derivatives via Electrophilic Amination
Gmeiner, Peter,Bollinger, Bernd
, p. 5927 - 5930 (2007/10/02)
A mild and efficient method for the construction of β-aryl amines from the corresponding α-aryl ketones is presented.The key step of the synthesis involve an electrophilic amination by dibenzyl azodicarboxylate followed by a stereoselective LiHBEt3 reduction.The reaction sequence is applied to the synthesis of the tricyclic ergoline analogue 4. Key words: electrophilic amination; stereoselective reduction; α-amino ketones.
