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Trichloroacetyl isocyanate

Trichloroacetyl isocyanate Structure
CAS No.
3019-71-4
Chemical Name:
Trichloroacetyl isocyanate
Synonyms
2,2,2-TRICHLOROACETYL ISOCYANATE;trichloroethanecarbonyl isocyanate;Trichloroacetyl isocyate;trichloro-acetylisocyanat;TRICHLOROACETYL ISOCYANATE;Acetyl isocyanate, trichloro-;Trichloroacetyl isocyanate ,97%;Trichloroacetyl isocyanate, GC 97%;Acetyl isocyanate, 2,2,2-trichloro-;Isocyanic Acid Trichloroacetyl Ester
CBNumber:
CB1337310
Molecular Formula:
C3Cl3NO2
Molecular Weight:
188.4
MOL File:
3019-71-4.mol
MSDS File:
SDS
Modify Date:
2024/7/8 20:25:11

Trichloroacetyl isocyanate Properties

Melting point 135-140 °C
Boiling point 80-85 °C/20 mmHg (lit.)
Density 1.581 g/mL at 25 °C (lit.)
refractive index n20/D 1.480(lit.)
Flash point 150 °F
storage temp. 2-8°C
solubility Miscible with dichloromethane, ether, terahydrofuran and protic solvents.
form Liquid
color Clear colorless to slightly yellow
Water Solubility Decomposition
Sensitive Moisture Sensitive
BRN 971201
Stability Hygroscopic, Moisture Sensitive
InChIKey GRNOZCCBOFGDCL-UHFFFAOYSA-N
CAS DataBase Reference 3019-71-4(CAS DataBase Reference)
NIST Chemistry Reference Trichloroacetyl isocyanate(3019-71-4)
EPA Substance Registry System Acetyl isocyanate, trichloro- (3019-71-4)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS05,GHS06,GHS08
Signal word  Danger
Hazard statements  H311+H331-H314-H317-H334
Precautionary statements  P261-P271-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338
Hazard Codes  T
Risk Statements  14-23/24-34-42-23/24/25-36/37/38
Safety Statements  23-26-36/37/39-45-8-7/9
RIDADR  UN 2206 6.1/PG 3
WGK Germany  3
10-19
TSCA  Yes
HazardClass  6.1
PackingGroup  II
HS Code  29291090
NFPA 704
2
3 0
W

Trichloroacetyl isocyanate price More Price(10)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 91095 Trichloroacetyl isocyanate purum, ≥97.0% (GC) 3019-71-4 5ML ₹8995.58 2022-06-14 Buy
Sigma-Aldrich(India) 91095 Trichloroacetyl isocyanate purum, ≥97.0% (GC) 3019-71-4 25ML ₹34921.45 2022-06-14 Buy
Sigma-Aldrich(India) 217328 Trichloroacetyl isocyanate 96% 3019-71-4 1G ₹1558.8 2022-06-14 Buy
Sigma-Aldrich(India) 217328 Trichloroacetyl isocyanate 96% 3019-71-4 10G ₹6917.18 2022-06-14 Buy
TCI Chemicals (India) T1047 Trichloroacetyl Isocyanate 3019-71-4 1G ₹1900 2022-05-26 Buy
Product number Packaging Price Buy
91095 5ML ₹8995.58 Buy
91095 25ML ₹34921.45 Buy
217328 1G ₹1558.8 Buy
217328 10G ₹6917.18 Buy
T1047 1G ₹1900 Buy

Trichloroacetyl isocyanate Chemical Properties,Uses,Production

Chemical Properties

clear colorless to slightly yellow liquid

Uses

Trichloroacetyl isocyanate was used in catalytic one-pot dehydrative glycosylation of 1-hydroxy carbohydrate. It was also used as a reagent for the conversion of alcohols to carbamates.

Application

Trichloroacetyl Isocyanate is used as an in situ derivatizing reagent for characterization of alcohols, glycols, phenols, and amines by nuclear magnetic resonance (NMR).It has been reported in the literature that it can be used for the preparation of cefuroxime axetil.

Preparation

Trichloroacetyl isocyanate can be obtained by reacting 2,2,2-trichloroacetamide with oxalyl chloride.
Procedure: A reaction mixture of 2,2,2-trichloroacetamide (100 g, 616 mmol, 1.0 eq) in (COCl)2 (725 g, 5.71 mol, 500 mL, 9.28 eq) was heated to 70°C for 24 hours. The reaction mixture was concentrated under vacuum. To the mixture was added 1,2,4-trichlorobenzene (500 mL) and (COCl)2 (116 g, 914 mmol, 80 mL, 1.48 eq). The reaction mixture was stirred at 100°C for 5 hours. Heat to 125°C for 15 hours. The mixture was then heated to 140°C for 5 hours. The reaction mixture was distilled under water pump (72°C-76°C fractions) to give trichloroacetyl isocyanate (60 g, 319 mmol, 52% yield) as a colorless oil.

General Description

Conformational stability and vibrational IR and Raman spectra of trichloroacetyl isocyanate has been investigated. Trichloroacetyl isocyanate is commonly employed as in situ derivatizing reagent for the 13C NMR studies of alcohols, phenols and amines. It undergoes 1,5-cycloaddition reaction with anhydro-2-deoxy-D-erythro- and -L-threo-pent-1-enitols and 1,5-anhydro-2-deoxy-D- and -L-arabino-hex-1-enitols to yield [2+2] and [4+2] cycloadducts.

Trichloroacetyl isocyanate Preparation Products And Raw materials

Global( 165)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
Anshul Chemicals Ltd. 91-22-28724091 / 28720854 New Delhi, India 27 39 Inquiry
TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6778 58 Inquiry
Alfa Aesar 1 800 209 7001 Maharashtra, India 6913 58 Inquiry
Merck Life Science Private Limited 08046045443 Mumbai, India 101 58 Inquiry
Anshul Specialty Molecules Private Limited 08066085867Ext 652 Mumbai, India 11 58 Inquiry
Anshul Specialty Molecules Pvt Ltd 08048372472Ext 403 Mumbai, India 9 58 Inquiry
A.J Chemicals 91-9810153283 New Delhi, India 6124 58 Inquiry
CLEARSYNTH LABS LTD. +91-22-45045900 Hyderabad, India 6351 58 Inquiry
CHEMSWORTH +91-261-2397244 New Delhi, India 6707 30 Inquiry
Oceanic Pharmachem Pvt., Ltd. (OPPL) 91-22-42128600 Maharashtra, India 947 58 Inquiry
Trichloroacetyl isocyate TRICHLOROACETYL ISOCYANATE Acetyl isocyanate, trichloro- trichloro-acetylisocyanat Trichloroacetyl isocyanate, NMR grade Isocyanic Acid Trichloroacetyl Ester Trichloroacetyl isocyanate, GC 97% Trichloroacetyl isocyanate ,97% 1-Oxo-2,2,2-trichloroethyl isocyanate Trichloroacetyl isocyanate, NMR grade 10GR TRICHLOROACETYL ISOCYANATE FOR SYNTHESIS Trichloroacetyl isocyanate puruM, >=97.0% (GC) Trichloroacetyl Isocyanate, 98.0%(N) Acetyl isocyanate, 2,2,2-trichloro- 2,2,2-TRICHLOROACETYL ISOCYANATE trichloroethanecarbonyl isocyanate 3019-71-4 C3Cl3NO2 Cl3CCONCO Isocyanates Nitrogen Compounds Organic Building Blocks Building Blocks Organics Isocyanates Nitrogen Compounds Organic Building Blocks Building Blocks Chemical Synthesis Nitrogen Compounds Organic Building Blocks