78152-12-2

Basic information

• Product Name: Carbonic acid, 4-(chlorocarbonyl)phenyl methyl ester (9CI)
• Synonyms: Carbonic acid, 4-(chlorocarbonyl)phenyl methyl ester (9CI)
• CAS NO: 78152-12-2
• Molecular Formula: C₉H₇ClO₄
• Molecular Weight: 214.60248
• Product Categories: ACIDHALIDE
• Mol File: 78152-12-2.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Carbonic acid, 4-(chlorocarbonyl)phenyl methyl ester (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Carbonic acid, 4-(chlorocarbonyl)phenyl methyl ester (9CI)(78152-12-2)
• EPA Substance Registry System: Carbonic acid, 4-(chlorocarbonyl)phenyl methyl ester (9CI)(78152-12-2)

Safety Data

• Hazardous Substances Data: 78152-12-2(Hazardous Substances Data)

Upstream product

• 99-96-7 4-hydroxy-benzoic acid 
• 14180-11-1 4-(methoxycarbonyloxy)benzoic acid 

Downstream Products

• 1034766-69-2 (3S,7S,10S)-10-(4'-methoxycarbonyloxybenzoyloxy)-3,7-dimethyl-5,8-dioxaundecan-6,9-dione 
• 344920-01-0 C₁₉H₂₆O₅ 
• 70568-45-5 4-n-heptyloxyphenyl 4-hydroxybenzoate 
• 345960-38-5 3,4-Bis-dodecyloxy-benzoic acid 4-[4-([1,4,7]dithiazonane-7-carbonyl)-phenoxycarbonyl]-phenyl ester 
• 345960-43-2 [7-(4-hydroxy-benzoyl)-[1,4,7]thiadiazonan-4-yl]-(4-hydroxy-phenyl)-methanone 
• 345960-41-0 [1,4,7]dithiazonan-7-yl-(4-hydroxy-phenyl)-methanone 

Relevant articles and documents

Synthesis of deuterium-labelled, optically active, ferroelectric liquid crystals

The synthesis of two selectively deuterium-labelled 4-(((S)-1-((S)-1-((S)-2-methylbutoxy)-1-oxopropan-2-yloxy)-1-oxopropan-2-yloxy)carbonyl)phenyl 4′-(heptyloxy)biphenyl-4-carboxylate derivatives is reported. A new preparation strategy was developed in or

Thermotropic liquid crystals from planar chiral compounds: [2.2]Paracyclophane as a mesogen core

New thermotropic mesomorphic compounds containing a [2.2]paracyclophane (PC) unit were synthesized and investigated (Scheme). Carboxylic acids were selected as the starting PC building blocks. The influence of structural features on the stability of the m

A Protection-Deprotection Method for the Synthesis of Substituted Benzoyloxybenzoates

Common syntheses of phenyl benzoyloxybenzoates generally produce products in low yields.A variety of synthetic pathways were employed in an attempt to increase the overall yield of the final product.It was found that catalytic agents such as boron trifluo