114326-14-6

Basic information

• Product Name: (3-CHLORO-PROPYL)-METHYL-CARBAMIC ACID TERT-BUTYL ESTER
• Synonyms: (3-CHLORO-PROPYL)-METHYL-CARBAMIC ACID TERT-BUTYL ESTER;N-Boc-N-Methyl-3-chloro-1-propanaMine;tert-Butyl (3-chloropropyl)(methyl)carbamate;Carbamic acid,N-(3-chloropropyl)-N-methyl-, 1,1-dimethylethyl ester
• CAS NO: 114326-14-6
• Molecular Formula: C₉H₁₈ClNO₂
• Molecular Weight: 207.69772
• Mol File: 114326-14-6.mol
• Article Data: 9

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (3-CHLORO-PROPYL)-METHYL-CARBAMIC ACID TERT-BUTYL ESTER(CAS DataBase Reference)
• NIST Chemistry Reference: (3-CHLORO-PROPYL)-METHYL-CARBAMIC ACID TERT-BUTYL ESTER(114326-14-6)
• EPA Substance Registry System: (3-CHLORO-PROPYL)-METHYL-CARBAMIC ACID TERT-BUTYL ESTER(114326-14-6)

Safety Data

• Hazardous Substances Data: 114326-14-6(Hazardous Substances Data)

Usage

General Description

"(3-Chloro-Propyl)-Methyl-Carbamic Acid Tert-Butyl Ester" is a chemical compound that is generally used in organic synthesis, pharmaceuticals, agrochemicals, and dyestuff fields. The structure of this chemical is characterized by a carbamic acid group attached to a propyl chain with a chloride, and a tert-butyl ester group. Its molecular formula can be represented as C8H16ClNO2. Safety and handling measures should be taken into consideration when using this compound, since some of its potential hazards could include being harmful if inhaled or swallowed, as well as causing skin irritation and serious eye damage.

Upstream product

• 116861-31-5 tert-butyl N-(3-chloropropyl)carbamate 
• 74-88-4 methyl iodide 
• 65232-62-4 methyl-3-chloropropylamine 
• 24424-99-5 di-tert-butyl dicarbonate 
• 114326-13-5 N-methyl-N-(tert-butoxycarbonyl)propanolamine tert-butyldimethylsilyl ether 
• 114326-12-4 [3-(tert-butyldimethylsilanyloxy)propyl]carbamic acid tert-butyl ester 
• 58885-58-8 N-tert-butoxycarbonyl-3-aminopropanol 
• 97145-88-5 3-chloro-N-methylpropan-1-amine hydrochloride 
• 98642-44-5 tert-butyl (3-hydroxypropyl)methylcarbamate 

Downstream Products

• 1240044-64-7 C₂₃H₂₅Cl₂N₃O₄ 
• 1516900-20-1 C₂₁H₃₂N₃O₂⁽¹⁺⁾*Cl^(1-) 
• 1421228-90-1 C₂₅H₂₉NO₆ 
• 114325-83-6 Methyl-[3-(2-oxo-2-phenyl-ethylsulfanyl)-propyl]-carbamic acid tert-butyl ester 

Relevant articles and documents

Synthesis and antiproliferative activity of marine bromotyrosine purpurealidin I and its derivatives

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Rapid and sensitive fluorescent probes for monoamine oxidases B to A at low concentrations

A new monoamine oxidase (MAO) fluorescent probe that displays response for both monoamine oxidase type-A (MAO-A) and monoamine oxidase type-B (MAO-B) is reported. This sensing platform does not require any additional enzymes or reagents. Furthermore, the

Substituted Indole Compounds

Substituted indole compounds corresponding to the formula I: In which R8, R9a, R9b, R10, R11, R200, R210, A, D, T, q, s and t have defined meanings, processes for the preparation thereof, pharmaceutical compositions containing such compounds and the use of substituted indole compounds for the treatment or inhibition of pain and other conditions which are at least partly mediated by Bradykinin 1 receptors (B1R).