122313-76-2 Usage
Uses
Used in Perfume and Fragrance Industry:
2,6-Octadien-1-ol, 3,7-dimethyl-, phenylcarbamate, (2Z)is used as a key ingredient in the production of perfumes and fragrances for its distinctive floral, herbal, and fruity scent. Its unique aroma profile contributes to the creation of various fragrance compositions, enhancing the overall sensory experience of the products.
Used in Pharmaceutical and Fine Chemical Synthesis:
Z-Carbamate plays a crucial role in the synthesis of pharmaceuticals and other fine chemicals. Its chemical properties make it a valuable intermediate in the production of various compounds, contributing to the development of new drugs and specialty chemicals.
Used as a Flavoring Agent in Food and Beverages:
In the food and beverage industry, 2,6-Octadien-1-ol, 3,7-dimethyl-, phenylcarbamate, (2Z)is utilized as a flavoring agent to impart specific taste profiles to products. Its fruity and herbal notes can enhance the flavor of various food items and beverages, providing a unique taste experience for consumers.
Used in Safety and Regulatory Compliance:
Given its potential as a fragrance sensitizer and allergen, Z-Carbamate is also used in the development and implementation of safety guidelines and regulatory compliance measures. Manufacturers and formulators must ensure that the handling and use of 2,6-Octadien-1-ol, 3,7-dimethyl-, phenylcarbamate, (2Z)- adhere to established safety protocols to minimize the risk of allergic reactions and sensitization.
Check Digit Verification of cas no
The CAS Registry Mumber 122313-76-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,3,1 and 3 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 122313-76:
(8*1)+(7*2)+(6*2)+(5*3)+(4*1)+(3*3)+(2*7)+(1*6)=82
82 % 10 = 2
So 122313-76-2 is a valid CAS Registry Number.
122313-76-2Relevant academic research and scientific papers
Oestreich, Martin,Auer, Gertrud
, p. 637 - 640 (2005)
The first copper-catalyzed allylic substitution reactions of allylic acetates and carbamates employing a bis(triorganosilyl)zinc reagent are reported. This novel procedure avoids the use of stoichiometric amounts of copper salts which are usually mandatory with this chemistry. Application of this methodology to standard model substrates substantiates a high diastereoselectivity for the double bond geometry (E:Z) as well as the relative configuration (syn:anti).
Catalytic Olefin Hydroamidation Enabled by Proton-Coupled Electron Transfer
Miller, David C.,Choi, Gilbert J.,Orbe, Hudson S.,Knowles, Robert R.
supporting information, p. 13492 - 13495 (2015/11/09)
Here we report a ternary catalyst system for the intramolecular hydroamidation of unactivated olefins using simple N-aryl amide derivatives. Amide activation in these reactions occurs via concerted proton-coupled electron transfer (PCET) mediated by an excited state iridium complex and weak phosphate base to furnish a reactive amidyl radical that readily adds to pendant alkenes. A series of H-atom, electron, and proton transfer events with a thiophenol cocatalyst furnish the product and regenerate the active forms of the photocatalyst and base. Mechanistic studies indicate that the amide substrate can be selectively homolyzed via PCET in the presence of the thiophenol, despite a large difference in bond dissociation free energies between these functional groups.
