36844-51-6

Basic information

• Product Name: 4-Allyloxybenzoyl chloride
• Synonyms: 4-Allyloxybenzoyl chloride;4-Allyloxybenzoyl chloride,98%
• CAS NO: 36844-51-6
• Molecular Formula: C₁₀H₉ClO₂
• Molecular Weight: 196.63026
• Mol File: 36844-51-6.mol
• Article Data: 28

Chemical Properties

• Appearance: Pink, orange-reddish/Low Melting Solid
• Storage Temp.: Freezer (-20°C)
• CAS DataBase Reference: 4-Allyloxybenzoyl chloride(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Allyloxybenzoyl chloride(36844-51-6)
• EPA Substance Registry System: 4-Allyloxybenzoyl chloride(36844-51-6)

Safety Data

• Hazardous Substances Data: 36844-51-6(Hazardous Substances Data)

Usage

Chemical Properties

Pink, orange-reddish low melting solid

Upstream product

• 27914-60-9 4-allyloxybenzoic acid 
• 5443-37-8 ethyl 4-(n-prop-2'-enyloxy)benzoate 
• 120-47-8 Ethyl 4-hydroxybenzoate 
• 99-96-7 4-hydroxy-benzoic acid 

Downstream Products

• 83953-73-5 cholesteryl 4-(2-propenyloxy)benzoate 
• 69819-27-8 4-allyloxy-N-(5-nitro-thiazol-2-yl)-benzamide 
• 42403-77-0 (4-(allyloxy)phenyl)(phenyl)methanone 

Relevant articles and documents

Mesomorphic properties of chiral three-arm liquid crystals containing 1,2,4-butanetriol as core

A series of symmetric and asymmetric three-arm liquid crystals (TALCs) of which the molecular structure with a central core of 1, 2, 4-butanetriol attached by three rod-like mesogenic moieties have successfully been synthesized. The rod-like mesogenic sid

Modified allyl compound, modified bismaleimide prepolymer and application thereof

The present invention provides a modified allyl compound, a modified bismaleimide prepolymer and application thereof, the modified allyl compound is represented by a formula (1), the modified allyl compound has a cyclopentadiene structure represented by a

Novel domino synthesis of 2-(2,3.4-substituted phenyl) quinazolin-4-amine

Convenient domino protocol was developed for the synthesis of 2-arylquinazolin-4-amines by the reaction of N-(2-cyanophenyl) substituted benzimidoyl isothiocyanates with isopropyl amine. The major advantages of this protocol are short reaction times, mild conditions, simple work up, high yields, and pure products. The efficacy of this protocol owes to the competence of synthesis, pure isolation of imidoyl isothiocyanates, and the unique structure conformation of the corresponding intermediate thiourea derivatives.