170230-01-0

Basic information

• Product Name: 4-Bromo-n-methoxy-n,3-dimethylbenzamide
• CAS NO: 170230-01-0
• Molecular Formula: C₁₀H₁₂BrNO₂
• Molecular Weight: 257.01
• Mol File: 170230-01-0.mol

Chemical Properties

• CAS DataBase Reference: 4-Bromo-n-methoxy-n,3-dimethylbenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Bromo-n-methoxy-n,3-dimethylbenzamide(170230-01-0)
• EPA Substance Registry System: 4-Bromo-n-methoxy-n,3-dimethylbenzamide(170230-01-0)

Safety Data

• Hazardous Substances Data: 170230-01-0(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
4-Bromo-n-methoxy-n,3-dimethylbenzamide serves as a valuable intermediate in organic synthesis, particularly for the preparation of other benzamide derivatives and related compounds. Its unique structure allows for further functionalization and modification, making it a versatile building block in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4-Bromo-n-methoxy-n,3-dimethylbenzamide is utilized as a research chemical for the development of new pharmaceutical agents. Its specific structural features may confer biological activities that can be harnessed for therapeutic purposes, such as modulating enzyme activity, receptor binding, or other pharmacological targets.
Used in Pharmaceutical Applications:
Although further studies are required to fully understand its potential, 4-Bromo-n-methoxy-n,3-dimethylbenzamide may have pharmaceutical applications as a lead compound for drug discovery. Its unique chemical structure could be optimized to develop new drugs with improved efficacy, selectivity, and safety profiles for the treatment of various diseases and conditions.

Upstream product

• 7697-28-1 4-bromo-3-methylbenzoic acid 
• 6638-79-5 N,O-dimethylhydroxylamine*hydrochloride 
• 21900-25-4 4-bromo-3-methylbenzoyl chloride 
• 148547-19-7 4-Bromo-3-methylbenzoic acid methyl ester 
• 1117-97-1 N,0-dimethylhydroxylamine 
• 13939-06-5 molybdenum hexacarbonyl 
• 68837-59-2 4-bromo-2-methylbenzoic acid 

Downstream Products

• 210228-01-6 1-(4-Bromo-3-methyl phenyl)-propan-1-one 
• 934464-36-5 1-(4'-chloro-2-methyl-biphenyl-4-yl)-ethanone 
• 644984-80-5 4-(4-bromo-3-methyl-phenyl)-3-methyl-4-oxo-butyric acid methyl ester 
• 644985-05-7 4-[4-(2-benzyl-3-oxo-cyclohex-1-enylamino)-3-methyl-phenyl]-3-methyl-4-oxo-butyric acid methyl ester 
• 871253-50-8 1-(4-bromo-3-methyl-phenyl)-5-methyl-hexan-1-one 
• 37074-40-1 1-(4-bromo-3-methylphenyl)ethan-1-one 
• 1125812-32-9 (2E/Z)-1-(4-bromo-3-methylphenyl)-4,4,4-trifluoro-3-(methoxymethylamino)-2-buten-1-one 
• 1125812-65-8 (2E/Z)-3-[bis(1-methylethyl)amino]-1-(4-bromo-3-methylphenyl)-4,4,4-trifluoro-2-buten-1-one 
• 1253045-42-9 C₁₃H₁₅BrO 
• 1321848-43-4 C₁₅H₂₁BO₃ 
• 1321848-45-6 C₁₇H₁₇NO₂ 
• 1321848-53-6 C₁₇H₁₅Br₂NO₂ 

Relevant articles and documents

Discovery of a Novel Potent and Selective Calcium Release-Activated Calcium Channel Inhibitor: 2,6-Difluoro- N-(2′-methyl-3′-(4-methyl-5-oxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)-[1,1′-biphenyl]-4-yl)benzamide. Structure-Activity Relationship and Preclinical Characterization

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PIPERIDINE COMPOUNDS AS PCSK9 INHIBITORS

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Mo(CO)6 as a Solid CO Source in the Synthesis of Aryl/Heteroaryl Weinreb Amides under Microwave-Enhanced Condition

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NOVEL INHIBITORS OF HEPATITIS C VIRUS

The invention provides compounds of formula (I): wherein the variables are defined in the specification, or a pharmaceutically-acceptable salt thereof, that are inhibitors of replication of the hepatitis C virus. The invention also provides pharmaceutical compositions comprising such compounds, methods of using such compounds to treat hepatitis C viral infections, and processes and intermediates useful for preparing such compounds.

HEPATITIS C INHIBITOR COMPOUNDS

Compounds of Formula (I): wherein R1, R2, RA, RB, Z1, Z2, Z3, Z4, Z5 and Z6 are defined herein. The compounds are useful as inhibitors of the function of NS5A protein encoded by HCV for the treatment of hepatitis C viral infection.

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METHOD FOR PREPARING 5-HALOALKYL-4,5-DIHYDROISOXAZOLE DERIVATIVES

Disclosed is a method for preparing a compound of Formula: (1); wherein R1 is CHX2, CX3, CX2CHX2 or CX2CX3; each X is independently Cl or F; Z is optionally substituted phenyl; and Q is phenyl or 1-naphthalenyl, each optionally substituted as defined in the disclosure; comprising contacting a compound of Formula: (2).

PYRAZOLINES FOR CONTROLLING INVERTEBRATE PESTS

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Benzimidazole derivatives bearing substituted biphenyls as hepatitis C virus NS5B RNA-dependent RNA polymerase inhibitors: Structure-activity relationship studies and identification of a potent and highly selective inhibitor JTK-109

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