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833-04-5

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Chemical structure

The compound consists of an indole ring with a bromine atom at the 5th position, and a 2-methylpropan-2-amine group attached to the 1st position of the indole ring.

Classification

It is a substituted amphetamine, which means it is a derivative of amphetamine with additional substituents on the amine group.

Psychoactive potential

Due to its structural similarity to other amphetamine compounds, it may have potential psychoactive or pharmacological effects.

Research interest

This chemical may be of interest to researchers and pharmacologists studying the effects and interactions of substituted amphetamines in the brain and body.

Molecular weight

Approximately 266.19 g/mol (based on the molecular formula)

Appearance

The compound is likely to be a solid, although specific information about its appearance is not provided in the material.

Solubility

The solubility of the compound is not mentioned in the material, but it may be soluble in organic solvents like ethanol or methanol due to its amine and indole groups.

Stability

Information about the stability of the compound is not provided in the material, but it may be sensitive to light, heat, or moisture, as is common with many organic compounds.

Synthesis

The synthesis of 1-(5-bromo-1H-indol-3-yl)-2-methylpropan-2-amine is not described in the material, but it likely involves the formation of the indole ring, bromination at the 5th position, and subsequent attachment of the 2-methylpropan-2-amine group.

Legal status

The legal status of this compound may vary by country, as it is a research chemical with potential psychoactive effects. It is important to be aware of and follow local regulations regarding the possession and use of such compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 833-04-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 833-04:
(5*8)+(4*3)+(3*3)+(2*0)+(1*4)=65
65 % 10 = 5
So 833-04-5 is a valid CAS Registry Number.

833-04-5SDS

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 1-(5-bromo-1H-indol-3-yl)-2-methylpropan-2-amine

1.2 Other means of identification

Product number -
Other names -

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:833-04-5 SDS

833-04-5Relevant articles and documents

Antihypertensive indole derivatives of phenoxypropanolamines with β-adrenergic receptor antagonist and vasodilating activity

Kreighbaum,Matier,Dennis,Minielli,Deitchman,Perhach Jr.,Comer

, p. 285 - 289 (2007/10/02)

A series of 25 aryloxypropanolamines containing the 3-indolyl-tert-butyl[i.e., 1,1-dimethyl-2-(1H-indol-3-yl)ethyl] or substituted 3-indolyl-tert-butyl moiety as the N substituent is reported. These compounds have been tested for antihypertensive activity in spontaneously hypertensive rats (SHR), β-adrenergic receptor antagonist action in conscious normotensive rats, vasodilating activity in ganglion-blocked rats with blood pressure maintained by angiotensin II infusion, and for intrinsic sympathomimetic action (ISA) in reserpinized rats. Some of the compounds exhibit antihypertensive activity in combination with β-adrenergic receptor antagonist and vasodilating action. The structure-activity relationships in these tests are discussed.

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