76875-23-5 Usage
Description
(E)-HEPT-2-ENOYL CHLORIDE, also known as trans-Hept-2-enoyl chloride, is a chemical compound with the formula C7H11ClO. It is a colorless liquid with a pungent odor and is a reactive compound commonly used in organic synthesis. It is primarily used as an intermediate in the production of various chemical compounds, including pharmaceuticals, agrochemicals, and fragrances. (E)-HEPT-2-ENOYL CHLORIDE is a valuable building block in the synthesis of carotenoids and other natural products. It is commonly used as a reactant in the preparation of esters, amides, and other functionalized compounds. Additionally, it is also utilized as a reagent in the production of polymers and other industrial chemicals. Overall, (E)-HEPT-2-ENOYL CHLORIDE is a versatile and important compound in the field of organic chemistry.
Uses
Used in Pharmaceutical Industry:
(E)-HEPT-2-ENOYL CHLORIDE is used as an intermediate for the synthesis of various pharmaceutical compounds. It plays a crucial role in the development of new drugs and medicines due to its ability to react with other compounds and form functionalized products.
Used in Agrochemical Industry:
(E)-HEPT-2-ENOYL CHLORIDE is used as a building block in the production of agrochemicals. Its reactivity allows for the creation of compounds that can be used in the development of pesticides, herbicides, and other agricultural products to improve crop yield and protect plants from pests.
Used in Fragrance Industry:
(E)-HEPT-2-ENOYL CHLORIDE is used as a reactant in the preparation of fragrances. Its ability to form esters and amides makes it a valuable component in the creation of various scent compounds used in the perfume and fragrance industry.
Used in Carotenoid Synthesis:
(E)-HEPT-2-ENOYL CHLORIDE is used as a building block in the synthesis of carotenoids, which are organic pigments found in plants, algae, and photosynthetic bacteria. These pigments are important for their antioxidant, anti-inflammatory, and photoprotective properties, and are used in the food, cosmetic, and pharmaceutical industries.
Used in Polymer Production:
(E)-HEPT-2-ENOYL CHLORIDE is used as a reagent in the production of polymers and other industrial chemicals. Its versatility in organic synthesis allows for the creation of a wide range of polymers with various properties and applications, contributing to the development of new materials and products in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 76875-23-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,8,7 and 5 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76875-23:
(7*7)+(6*6)+(5*8)+(4*7)+(3*5)+(2*2)+(1*3)=175
175 % 10 = 5
So 76875-23-5 is a valid CAS Registry Number.
76875-23-5Relevant articles and documents
Synthesis of β,γ-unsaturated primary amides from α,β-unsaturated acids and investigation of the mechanism
Theodorou, Vassiliki,Gogou, Marina,Philippidou, Maria,Ragoussis, Valentine,Paraskevopoulos, Georgios,Skobridis, Konstantinos
experimental part, p. 5630 - 5634 (2011/08/22)
α,β-Unsaturated acids, through their acid chlorides, react with tritylamine in the presence of triethylamine under mild conditions, to afford in high yield and high regioselectivity the corresponding β,γ- unsaturated tritylamides. Detritylation with TFA generates quantitatively β,γ-unsaturated primary amides. An investigation of this deconjugative isomerization was performed.
Dispiroketals in synthesis (Part 16): Functionalised dispiroketals as new chiral auxiliaries; the synthesis of dihydroxylated dispiroketals in optically pure form and their application as bifunctional , C2-symmetrical, chiral auxiliaries for highly stereoselective Michael additions
Bezuidenhoudt, Barend C. B.,Castle, Grant H.,Innes, Jean E.,Ley, Steven V.
, p. 184 - 194 (2007/10/02)
A range of rigid, architecturally complex diols derived from dispiroketals have been synthesised.A bifunctional, C2-symmetrical, chiral auxiliary derived from these dihydroxylated dispiroketals has been used to induce a high degree of asymmetry in Michael additions of cuprates to a variety of di-α,β-unsaturated ester systems.