98074-64-7 Usage
Description
(1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-YL)-HYDRAZINE is a chemical compound derived from naphthalene and hydrazine. It is a colorless liquid with a faint odor and is used as a raw material for the synthesis of various chemical compounds.
Used in Pharmaceutical Industry:
(1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-YL)-HYDRAZINE is used as a raw material for the synthesis of pharmaceutical compounds due to its potential applications in the development of new drugs.
Used in Agrochemical Industry:
(1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-YL)-HYDRAZINE is used as a raw material for the synthesis of agrochemical compounds, contributing to the development of new pesticides and other agricultural chemicals.
Used in Dye Production:
(1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-YL)-HYDRAZINE is used as a raw material in the production of dyes, playing a role in the creation of various colorants for different applications.
Used in Polymer Production:
(1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-YL)-HYDRAZINE is used as a raw material in the production of polymers, contributing to the development of new materials with specific properties for various industries.
Safety Precautions:
It is important to handle (1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-YL)-HYDRAZINE with caution, as it can be hazardous if not used properly. (1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-YL)-HYDRAZINE should be stored in a cool, dry place away from heat, sparks, and open flame, and should be handled with appropriate protective equipment to minimize the risk of exposure.
Check Digit Verification of cas no
The CAS Registry Mumber 98074-64-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,0,7 and 4 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 98074-64:
(7*9)+(6*8)+(5*0)+(4*7)+(3*4)+(2*6)+(1*4)=167
167 % 10 = 7
So 98074-64-7 is a valid CAS Registry Number.
98074-64-7Relevant articles and documents
Stereoselective coupling of prochiral radicals with a chiral C2-symmetric nitroxide
Braslau, Rebecca,Naik, Neeta,Zipse, Hendrik
, p. 8421 - 8434 (2007/10/03)
The coupling reaction beween a chiral C2-symmetric nitroxide, trans-2,5-dimethyl-2,5-diphenylpyrrolidin-1-oxyl (DPPO; 1), and a series of stabilized secondary prochiral radicals was studied to determine the factors that affect stereoselectivity. Both steric and electronic perturbations on the selectivity by the substituents of the prochiral radical were observed. The effects of temperature, solvent polarity, and solvent viscosity were examined. High selectivity for reactions carried out in solvents of low viscosity provides evidence for the formation of an encounter complex on the reaction path. Ab initio calculations on simplified model systems predict the C-O-N angle of attack to be greater than 110°at a carbon-oxygen bond-forming distance of approximately 2.2 A, although no transition state was found.
