1447-14-9

Basic information

• Product Name: 2,2-DICHLORO-1-METHYLCYCLOPROPANECARBOXYLIC ACID
• Synonyms: 2,2-DICHLORO-1-METHYLCYCLOPROPANECARBOXYLIC ACID;LABOTEST-BB LT00452792;1-Methyl-2,2-dichlorocyclopropane-1-carboxylic acid;1-Methyl-2,2-dichlorocyclopropanecarboxylic acid;2,2-Dichloro-1-methyl-cyclopropanecarboxylic acid 98%;2,2-dichloro-1-methyl-1-cyclopropanecarboxylic acid
• CAS NO: 1447-14-9
• Molecular Formula: C₅H₆Cl₂O₂
• Molecular Weight: 169.01
• EINECS: 215-901-6
• Product Categories: C1 to C5;Carbonyl Compounds;Carboxylic Acids;Building Blocks;C1 to C5;Carbonyl Compounds;Carboxylic Acids;Chemical Synthesis;Organic Building Blocks
• Mol File: 1447-14-9.mol
• Article Data: 4

Chemical Properties

• Melting Point: 60-65 °C(lit.)
• Boiling Point: 85 °C8 mm Hg(lit.)
• Flash Point: 87.7°C
• Appearance: /
• Density: 1.3010 (estimate)
• Vapor Pressure: 0.135mmHg at 25°C
• Refractive Index: 1.53
• PKA: 3.51±0.50(Predicted)
• BRN: 1937304
• CAS DataBase Reference: 2,2-DICHLORO-1-METHYLCYCLOPROPANECARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2-DICHLORO-1-METHYLCYCLOPROPANECARBOXYLIC ACID(1447-14-9)
• EPA Substance Registry System: 2,2-DICHLORO-1-METHYLCYCLOPROPANECARBOXYLIC ACID(1447-14-9)

Safety Data

• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36
• RIDADR: 1760
• WGK Germany: 3
• HazardClass: 8
• PackingGroup: III
• Hazardous Substances Data: 1447-14-9(Hazardous Substances Data)

Usage

Uses

2,2-Dichloro-1-methyl-cyclopropanecarboxylic acid was used in solid phase synthesis of α-hydroxy esters, inhibitors of amyloid-β production.

InChI:InChI=1/C5H6Cl2O2/c1-4(3(8)9)2-5(4,6)7/h2H2,1H3,(H,8,9)

Upstream product

• 79-41-4 poly(methacrylic acid) 
• 67-66-3 chloroform 
• 5296-49-1 1-vinyl-1-methyl-2,2-dichlorocyclopropane 
• 563-41-7 semicarbazide hydrochloride 
• 56-37-1 N-benzyl-N,N,N-triethylammonium chloride 
• 292638-85-8 acrylic acid methyl ester 
• 35757-05-2 2,2-dichloro-1-methylcyclopropanecarbonitrile 
• 91772-23-5 2,2-Dichlor-1-methyl-1--cyclopropan 
• 35749-17-8 2,2-dichloro-1-methylcyclopropylcarboxamide 

Downstream Products

• 1447-13-8 methyl 2,2-dichloro-1-methylcyclopropanecarboxylate 
• 6914-76-7 1-Methyl-cyclopropanoic acid 
• 1354043-51-8 C₂₂H₁₈Cl₂FN₇O₂ 
• 4128-37-4 1,3-diisopropylurea 
• 1160842-94-3 4-phenylbutan-2-yl-2,2-dichloro-1-methylcyclopropanecarboxylate 
• 81513-11-3 hexyl-2,2-dichloro-1-methylcyclopropanecarboxylate 
• 1160842-86-3 phenethyl-2,2-dichloro-1-methylcyclopropanecarboxylate 
• 156819-60-2 2,2-dichloro-1-methylcyclopropyl carboxylic acid N'-[2,6-dichloro-4-(trifluoromethyl)phenyl]hydrazide 
• 132712-55-1 α(RS)-cyano-3-phenoxybenzyl 2,2-dichloro-1-methylcyclopropane-1-carboxylate 
• 132712-54-0 3-phenoxybenzyl 2,2-dichloro-1-methylcyclopropane-1-carboxylate 
• 137343-66-9 2,2-dichloro-1-methylcyclopropyl(phenyl)methanone 
• 701222-94-8 (-)-(R)-[(1S)-2,2-dichloro-1-methylcyclopropyl](2-chlorophenyl)(2-tolyl)methanol 
• 701222-83-5 (-)-(S)-[(1S)-2,2-dichloro-1-methylcyclopropyl](2-methoxyphenyl)(o-tolyl)methanol 
• 701222-89-1 (-)-(R)-[(1S)-2,2-dichloro-1-methylcyclopropyl](2-chlorophenyl)(2-methoxyphenyl)methanol 

Relevant articles and documents

A process for preparing 1-methyl propyl formic acid method

The invention discloses a method for preparing 1-methyl cyclopropane carboxylic acid and belongs to the fields of fine chemical engineering and medical intermediates. The method comprises the following steps: by taking methacrylic acid (ester or salt), or methacrylonitrile or methacrylamide as a raw material, carrying out a cyclopropanation reaction with trihalide in the presence of an alkali to generate 2,2-geminal halide (III); carrying out a reaction between the 2,2-geminal halide (III) and metallic sodium to remove halogen atoms on the ring so as to generate methyl cyclopropionate or methyl cyclopropaneacetonitrile or methyl cyclopropylamide (II); acidifying the methyl cyclopropanecarboxylate, thereby obtaining 1-methyl cyclopropane carboxylic acid (I); and performing basic hydrolysis on methyl cyclopropaneacetonitrile or methyl cyclopropylamide, and acidifying to obtain 1-methyl cyclopropane carboxylic acid (I). The method disclosed by the invention is readily available in raw materials, mild in reaction conditions, convenient to operate, low in cost and high in purity of the obtained product and is a feasible preparation method.

6-(Substituted-cycloalkylcarboxamide) penicillanic acids

Penicillins of the formula SPC1 Or a pharmaceutically-acceptable, nontoxic salt thereof, Wherein R1 and R2 are the same or different and each is hydrogen, fluorine, chlorine or bromine; or when R2 is hydrogen, R1 can also be cyano, hydroxyl, azido, amino or nitro; or R1 and R2 are bonded to a ring carbon atom and constitute a single oxygen atom; R3 is hydrogen, methyl, chlorine, bromine, cyano, methoxy or carboxyl; and n is 2 to 7; Are useful for their antibacterial activity.