794507-89-4 Usage
Uses
Used in Organic Synthesis:
(R)-7-broMo-1,2,3,4-tetrahydronaphthalen-1-aMine is utilized as a chemical intermediate in organic synthesis, playing a crucial role in the formation of various complex organic molecules.
Used in Pharmaceutical Production:
(R)-7-broMo-1,2,3,4-tetrahydronaphthalen-1-aMine serves as a key intermediate in the production of pharmaceuticals, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemicals:
(R)-7-broMo-1,2,3,4-tetrahydronaphthalen-1-aMine is also employed in the agrochemical industry, where it acts as a chemical intermediate for the synthesis of pesticides and other agrochemical products.
Used in Drug Development:
Due to its unique structural features and reactivity, (R)-7-broMo-1,2,3,4-tetrahydronaphthalen-1-aMine holds potential for use in the development of new drugs, offering novel therapeutic options for various medical conditions.
Used in Material Science:
(R)-7-broMo-1,2,3,4-tetrahydronaphthalen-1-aMine may also find applications in the field of material science, where it could be utilized in the creation of new materials with specific properties and applications.
It is important to handle and use (R)-7-broMo-1,2,3,4-tetrahydronaphthalen-1-aMine with proper precautions and in accordance with safety guidelines due to its reactivity and potential hazards.
Check Digit Verification of cas no
The CAS Registry Mumber 794507-89-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,4,5,0 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 794507-89:
(8*7)+(7*9)+(6*4)+(5*5)+(4*0)+(3*7)+(2*8)+(1*9)=214
214 % 10 = 4
So 794507-89-4 is a valid CAS Registry Number.
794507-89-4Relevant academic research and scientific papers
ION CHANNEL INHIBITOR COMPOUNDS FOR CANCER TREATMENT
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Paragraph 0223; 0224, (2021/01/25)
The present invention concerns a compound of following general formula (I): where: either R is an R1 group and R′ is an -A1-Cy1 group, or R is an -A1-Cy1 group and R′ is an R1 group, R1 particularly being H or (C1-C6)alkyl group;A1 being an —NH— radical or —NH—CH2— radical;Cy1 particularly being a phenyl group,A is a fused (hetero)aromatic ring having 5 to 7 atoms, for use for treating cancer.
Microwave-accelerated reductive amination between ketones and ammonium acetate
Dong, Li,Aleem, Saadat,Fink, Cynthia A.
experimental part, p. 5210 - 5212 (2010/11/05)
A new procedure for reductive amination between ketones and ammonium acetate has been developed to access a variety of primary amines. This protocol takes advantage of microwave heating to significantly accelerate the reaction and offers a convenient and effective method to access some interesting amines. This new procedure compares favorably to previously reported approaches in terms of practicality, efficiency, and functional group compatibility.
