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865472-04-4

7-Bromo-1,2,3,4-tetrahydro-naphthalen-1-ylamine hydrochloride is a chemical compound that is frequently utilized in research and experimentation. It is composed of elements such as bromine, hydrogen, nitrogen, and chlorine, and its properties, including stability and reactivity, can change under varying conditions like temperature and concentration. As with many chemicals of its kind, it requires careful handling and storage to ensure safety. Information regarding its toxicity and health effects is typically found in safety data sheets, which provide details based on known or evaluated data for human and environmental health. 7-BROMO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-YLAMINE HYDROCHLORIDE is particularly valued in the pharmaceutical industry due to its biologically active properties.

865472-04-4

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865472-04-4 Usage

Uses

Used in Pharmaceutical Industry:
7-BROMO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-YLAMINE HYDROCHLORIDE is used as a biologically active compound for the development of pharmaceutical products. Its unique chemical structure and properties make it a valuable component in the synthesis of various drugs and therapeutic agents. 7-BROMO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-YLAMINE HYDROCHLORIDE's potential applications in medicine are being explored and utilized to create new treatments and improve existing ones.

Check Digit Verification of cas no

The CAS Registry Mumber 865472-04-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,5,4,7 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 865472-04:
(8*8)+(7*6)+(6*5)+(5*4)+(4*7)+(3*2)+(2*0)+(1*4)=194
194 % 10 = 4
So 865472-04-4 is a valid CAS Registry Number.
InChI:InChI=1/C10H12BrN.ClH/c11-8-5-4-7-2-1-3-10(12)9(7)6-8;/h4-6,10H,1-3,12H2;1H

865472-04-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-bromo-1,2,3,4-tetrahydronaphthalen-1-amine

1.2 Other means of identification

Product number -
Other names 7-BROMO-1,2,3,4-TETRAHYDRO-NAPHTHALEN-1-YLAMINE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:865472-04-4 SDS

865472-04-4Downstream Products

865472-04-4Relevant articles and documents

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.

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