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1-propanamine, 2-methyl-, hydrobromide (1:1) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74098-36-5

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74098-36-5 Usage

Uses

Used in Pharmaceutical Industry:
1-propanamine, 2-methyl-, hydrobromide (1:1) is used as a component in medications for its potential therapeutic properties.
Used in Research Laboratories:
1-propanamine, 2-methyl-, hydrobromide (1:1) is used in research laboratories for organic synthesis, contributing to the development of new compounds and materials.
Used as a Reagent in Chemical Reactions:
1-propanamine, 2-methyl-, hydrobromide (1:1) serves as a reagent in various chemical reactions, facilitating specific transformations and processes.
Used as a Solvent in Organic Chemistry:
1-propanamine, 2-methyl-, hydrobromide (1:1) is utilized as a solvent in organic chemistry, enabling the dissolution and interaction of various organic compounds for research and synthesis purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 74098-36-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,0,9 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74098-36:
(7*7)+(6*4)+(5*0)+(4*9)+(3*8)+(2*3)+(1*6)=145
145 % 10 = 5
So 74098-36-5 is a valid CAS Registry Number.

74098-36-5Downstream Products

74098-36-5Relevant academic research and scientific papers

KINETICS AND MECHANISM OF REACTION OF AMINES WITH β-BROMOPROPIOPHENONE

Popov, A. F.,Piskunova, Z.,Matvienko, V. N.

, p. 1299 - 1302 (2007/10/02)

The reaction of β-bromopropiophenone with different amines in acetonitrile at 25 deg C was studied.It was found that in the case of primary and secondary amines, the end products of the reaction are β-aminopropiophenones, which form via the intermediate phenyl vinyl ketone.In the case of tertiary amines, the reaction ends at the stage of the formation of phenyl vinyl ketone.The reactivity of the amines in the formation of phenyl vinyl ketone is preferentially determined by their basicity.

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