94318-80-6

Basic information

• Product Name: 2-BROMO-N-TERT-BUTYL-PROPANAMIDE
• Synonyms: 2-BROMO-N-TERT-BUTYL-PROPANAMIDE;2-bromo-N-(tert-butyl)propanamide(SALTDATA: FREE)
• CAS NO: 94318-80-6
• Molecular Formula: C₇H₁₄BrNO
• Molecular Weight: 208.1
• Mol File: 94318-80-6.mol
• Article Data: 4

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-BROMO-N-TERT-BUTYL-PROPANAMIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BROMO-N-TERT-BUTYL-PROPANAMIDE(94318-80-6)
• EPA Substance Registry System: 2-BROMO-N-TERT-BUTYL-PROPANAMIDE(94318-80-6)

Safety Data

• Hazardous Substances Data: 94318-80-6(Hazardous Substances Data)

Usage

General Description

2-BROMO-N-TERT-BUTYL-PROPANAMIDE is a chemical compound with the molecular formula C7H14BrNO. It is a white solid at room temperature and is commonly used as a reagent in organic synthesis. 2-BROMO-N-TERT-BUTYL-PROPANAMIDE is used in the production of pharmaceuticals, agrochemicals, and various other industrial products. It is also utilized as a chemical intermediate in the manufacturing of other organic compounds. 2-BROMO-N-TERT-BUTYL-PROPANAMIDE is known for its ability to undergo various chemical reactions, making it a versatile and valuable compound in the field of organic chemistry.

Upstream product

• 75-64-9 tert-butylamine 
• 7148-74-5 2-Bromopropionyl chloride 
• 563-76-8 α-bromopropionyl bromide 
• 598-72-1 2-Bromopropionic acid 

Downstream Products

• 1192477-85-2 tert-butyl 3-((1-(tert-butylamino)-1-oxopropan-2-ylamino)methyl)benzylcarbamate 
• 1192477-15-8 [3-({(1-tert-butylcarbamoyl-ethyl)-[2-(1H-indol-3-yl)-2-oxo-acetyl]amino}methyl)benzyl]carbamic acid tert-butyl ester 
• 1192477-86-3 2-{(3-aminomethyl-benzyl)-[2-(1H-indol-3-yl)-2-oxo-acetyl]amino}-N-tert-butyl-propionamide 

Relevant articles and documents

Continuous-Flow Electrosynthesis of Benzofused S-Heterocycles by Dehydrogenative C?S Cross-Coupling

Reported herein is the synthesis of benzofused six-membered S-heterocycles by intramolecular dehydrogenative C?S coupling using a modular flow electrolysis cell. The continuous-flow electrosynthesis not only ensures efficient product formation, but also obviates the need for transition-metal catalysts, oxidizing reagents, and supporting electrolytes. Reaction scale-up is conveniently achieved through extended electrolysis without changing the reaction conditions and equipment.

CALCIUM ION CHANNEL MODULATORS and USES THEREOF

Compounds of formula (I), wherein R1 is hydrogen, hydroxyl or aralkyl; R2 is an optionally substituted alkyl, aryl or heteroaryl (said substituents are selected from hydroxyl, alkoxyl, haloalkoxyl, aryl, heteroaryl, cycloalkyl, amino, monoalkylamino, dialkylamino, alkylsulphonyl, alkylsulphinyl, alkylsulphonylamino, acylamino, saturated or partially unsaturated heterocyclic groups and groups of formula COY); W is selected from oxygen, sulphur, groups of formula NR7, wherein R7 is hydrogen, alkyl, aryl or heteroaryl and groups of formula CR8R9, wherein R8 and R9 are hydrogen, alkyl, aryl or heteroaryl; and X is selected from nitrogen and groups of formula CR10, wherein R10 is hydrogen, alkyl, aryl, heteroaryl, halogen or haloalkyl, inhibit the interaction between Cavx channels and Cavβ proteins and are of use in the treatment and prevention of a number of diseases and conditions including pain and lower urinary tract disorders.