37488-40-7 Usage
Description
BENZYLAMINE HYDROBROMIDE is an organic compound with the chemical formula C7H10BrN. It is a white crystalline solid that is soluble in water and has a characteristic amine-like odor. It is derived from benzylamine, where a hydrobromic acid molecule is added to form the hydrobromide salt. BENZYLAMINE HYDROBROMIDE is known for its reactivity and is used in various applications across different industries.
Uses
Used in Pharmaceutical Industry:
BENZYLAMINE HYDROBROMIDE is used as an intermediate in the synthesis of various pharmaceutical compounds for [application reason]. Its reactivity allows for the creation of a wide range of drugs with different therapeutic properties.
Used in Chemical Synthesis:
BENZYLAMINE HYDROBROMIDE is used as a reagent in chemical synthesis for [application reason]. Its ability to form salts and react with other compounds makes it a versatile building block for creating new molecules with specific functions.
Used in Research and Development:
BENZYLAMINE HYDROBROMIDE is used as a research compound for [application reason]. It is often utilized in laboratories to study its properties and to develop new methods for synthesizing related compounds or understanding its interactions with other molecules.
Used in Solar Cell Applications:
BENZYLAMINE HYDROBROMIDE is used as a precursor in the synthesis of organohalide-based perovskites for [application reason]. These perovskites are important materials for optimizing the band gap, carrier diffusion length, and power conversion efficiency of perovskite-based solar cells.
Check Digit Verification of cas no
The CAS Registry Mumber 37488-40-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,4,8 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 37488-40:
(7*3)+(6*7)+(5*4)+(4*8)+(3*8)+(2*4)+(1*0)=147
147 % 10 = 7
So 37488-40-7 is a valid CAS Registry Number.
37488-40-7Relevant articles and documents
Nucleophilic substitution reactions of N-methyl α-bromoacetanilides with benzylamines in dimethyl sulfoxide
Adhikary, Keshab Kumar,Lee, Hai Whang
scheme or table, p. 857 - 862 (2012/01/13)
Kinetic studies of the reactions of N-methyl-Y-a-bromoacetanilides with substituted X-benzylamines have been carried out in dimethyl sulfoxide at 25.0 °C. The Hammett plots for substituent X variations in the nucleophiles (log kN vs σX) are slightly bipha
KINETICS OF THE REACTIONS OF 2-HALOGENOPYRIDINIUM SALTS WITH PRIMARY AND SECONDARY AMINES IN ACETONITRILE
Litvinenko, L. M.,Titskii, G. D.,Mitchenko, E. S.
, p. 1731 - 1736 (2007/10/02)
The kinetics of the reactions of 2-halogeno-N-alkylpyridinium salts with primary and secondary aliphatic amines in acetonitrile at 25 deg C were investigated.The reactions obey second-order relationships.In the reaction of 2-bromo-N-ethylpyridinium bromide with aliphatic amines the effect of electronic and steric factors on the reactivity of the amines was examined.
