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Benzenemethanol, 3-bromo-4,5-dimethoxy-α-methyl-, also known as 3-bromo-4,5-dimethoxy-α-methylbenzenemethanol, is an organic compound with the chemical formula C10H13BrO2. It is a derivative of benzyl alcohol, featuring a benzene ring with a bromine atom at the 3-position, two methoxy groups at the 4 and 5 positions, and a methyl group at the α-carbon. Benzenemethanol, 3-bromo-4,5-dimethoxy-a-methyl- is characterized by its unique structure, which may have potential applications in the synthesis of pharmaceuticals, agrochemicals, or other specialty chemicals. Due to its specific functional groups, it can be involved in various chemical reactions, such as nucleophilic substitutions, eliminations, or condensations, making it a versatile building block in organic synthesis.

5293-21-0

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5293-21-0 Usage

Chemical compound

Benzenemethanol, 3-bromo-4,5-dimethoxy-α-methyl-

Also known as

3-Bromo-4,5-dimethoxy-α-methylbenzeneethanol

Derivative of

Methamphetamine

Belongs to class of

Phenethylamines

Structural features

Bromine atom, two methoxy groups, methyl group on alpha carbon

Properties

Potent hallucinogenic, psychoactive substance

Classification

Controlled or illegal drug in many countries

Effects on central nervous system

Altered perception, mood changes, hallucinations

Potential for

Abuse and dependence.

Check Digit Verification of cas no

The CAS Registry Mumber 5293-21-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,9 and 3 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5293-21:
(6*5)+(5*2)+(4*9)+(3*3)+(2*2)+(1*1)=90
90 % 10 = 0
So 5293-21-0 is a valid CAS Registry Number.

5293-21-0Relevant academic research and scientific papers

NOVEL MODULATORS OF PROTEIN KINASE SIGNALING

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Page/Page column 62, (2009/12/28)

The present invention provides new tyrphostin derivatives acting as protein kinase (PK) and receptor kinase (RK) signaling modulators. The invention further provides methods of their preparation, pharmaceutical compositions including such compounds, and m

Synthesis and structure-activity relationships of cephalosporins with C-3' catechol-containing residues

Arnould,Bertrandie,Bird,Boucherot,Jung,Lohmann,Olivier,Bailey,Bell,Davies

, p. 2631 - 2642 (2007/10/02)

Cephalosporins with new catechol substituents at C-3' have been synthesized, including novel compounds with C-3' carbon-carbon bonds. Many of these compounds have high potency against Gram-negative bacteria, in particular against resistant strains like Ps

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