260967-14-4

Basic information

• Product Name: (E)-benzyl prop-1-en-1-ylcarbamate
• Synonyms: (E)-benzyl prop-1-en-1-ylcarbamate;Carbamic acid, (1E)-1-propenyl-, phenylmethyl ester
• CAS NO: 260967-14-4
• Molecular Formula: C₁₁H₁₃NO₂
• Molecular Weight: 191.22642
• EINECS: -0
• Mol File: 260967-14-4.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 291.7±23.0 °C(Predicted)
• Appearance: /
• Density: 1.076±0.06 g/cm3(Predicted)
• PKA: 11.65±0.46(Predicted)
• CAS DataBase Reference: (E)-benzyl prop-1-en-1-ylcarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-benzyl prop-1-en-1-ylcarbamate(260967-14-4)
• EPA Substance Registry System: (E)-benzyl prop-1-en-1-ylcarbamate(260967-14-4)

Safety Data

• Hazardous Substances Data: 260967-14-4(Hazardous Substances Data)

Usage

General Description

(E)-Benzyl prop-1-en-1-ylcarbamate, also known as benzyl cinnamyl carbamate, is a chemical compound that belongs to the class of organic compounds known as cyclic carboximidic acids and derivatives. It is commonly used as a fragrance ingredient in cosmetics and personal care products, as well as in the production of food flavoring compounds. This chemical has a floral and sweet fragrance and is often added to perfumes, lotions, and soaps to give them a pleasant scent. However, it is also known to be a potential allergen and can trigger allergic reactions in some individuals. Therefore, it is important to use products containing this compound with caution.

Upstream product

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Relevant articles and documents

Lewis Acid Catalyzed [3+2] Coupling of Quinone Monoacetals or Quinone Imine Ketals with Vinylcarbamates

A mild and concise [3+2] coupling of quinone monoacetals or quinone imine ketals with vinylcarbamates promoted by Lewis acid was realized. Various 2-carbamate-2,3-dihydrobenzofurans and 2-carbamate-indolines have been prepared in moderate to good yields.

Structure-Dependent Nickel-Catalysed Transposition of N -Allylamides to E- or Z-Enamides

The nickel-catalysed transposition of a carbon-carbon double bond of N-allyl and N-homoallyl amides is described. While the transposition of acyclic amides gave very high Z-selectivity of the enamides, corresponding cyclic N-allyl amides led exclusively t

Nickel-Catalyzed Synthesis of Enamides and Enecarbamates via Isomerization of Allylamides and Allylcarbamates

A single-component, air-stable nickel precatalyst can catalyze the isomerization of allylamides for the synthesis of enamides. The scope of the reaction encompasses various substituted allylamides and allylcarbamates as well as homoallylamides. The reaction can be performed on a multigram-scale without specialized glove-box equipment or Schlenk techniques.