Methyl dichloroacetate

• Catalog No.: 108405
• CAS Number: 116-54-1
• M. F.: C3H4Cl2O2
• M. W.: 142.96866
• Purity: ≥99%

SYNONYMS

• Title: 二氯乙酸甲酯
• IUPAC name: methyl 2,2-dichloroacetate
• IUPAC Traditional name: methyl dichloroacetate
• Synonyms: NSC 2882; Dichloroacetic acid methyl ester

DATABASE IDS

• CAS Number: 116-54-1
• MDL Number: MFCD00000843
• Beilstein Number: 1747542
• EC Number: 204-146-8

PROPERTIES

• Linear Formula: Cl2CHCOOCH3
• Purity: ≥99%
• Boiling Point: 143 °C(lit.)
• Density: 1.381 g/mL at 25 °C(lit.)
• Flash Point: 64 °C
• Flash Point: 147.2 °F
• Melting Point: -52 °C(lit.)
• Refractive Index: n20/D 1.442(lit.)
• GHS Signal Word: Warning
• GHS Hazard statements: H315-H319-H332-H335
• European Hazard Symbols: Harmful (Xn)
• Personal Protective Equipment: Eyeshields, Faceshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
• GHS Precautionary statements: P261-P305 + P351 + P338
• RID/ADR: UN 2299 6.1/PG 3
• Risk Statements: 20-36/37/38
• RTECS: AG6625000
• Safety Statements: 26-36
• Hazard Class: 6.1
• UN Number: 2299
• Packing Group: 3
• German water hazard class: 3

DETAILS

Description (简体中文)

Application
Reactant involved in:
• Nucleophilic substitution reactions with nitro(pentafluorosulfanyl)benzenes1
• Azide-alkyl halide cycloaddition and atom transfer radical addition2
• Chemical modification of STn antigen for enhancement of synthetic carbohydrate vaccines3
• Three component reaction of arynes with cyclic ethers and active methines4
• Catalytic radical haloalkylation for synthesis of neodysidenin5
• Addition reactions for syntehsis of enantiopure 3,4-diamino esters or amides6

Description (English)

Application
Reactant involved in:
• Nucleophilic substitution reactions with nitro(pentafluorosulfanyl)benzenes1
• Azide-alkyl halide cycloaddition and atom transfer radical addition2
• Chemical modification of STn antigen for enhancement of synthetic carbohydrate vaccines3
• Three component reaction of arynes with cyclic ethers and active methines4
• Catalytic radical haloalkylation for synthesis of neodysidenin5
• Addition reactions for syntehsis of enantiopure 3,4-diamino esters or amides6