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1513-87-7

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1513-87-7 Usage

Preparation

A solution of 2,2,2-trifluoroethanol (200 g, 2.0 mol) and pyridine (158 g, 2.0 mol) in dry diethyl ether (1 L) was treated with phosgene (99 g, 1.0 mol). The reaction mixture was stirred overnight and then filtered. The filtrate was distilled to give 199 g (88%) of bis(2,2,2-trifluoroethyl) carbonate.

Check Digit Verification of cas no

The CAS Registry Mumber 1513-87-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,1 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1513-87:
(6*1)+(5*5)+(4*1)+(3*3)+(2*8)+(1*7)=67
67 % 10 = 7
So 1513-87-7 is a valid CAS Registry Number.

1513-87-7 Well-known Company Product Price

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  • TCI America

  • (B4703)  Bis(2,2,2-trifluoroethyl) Carbonate  >98.0%(GC)

  • 1513-87-7

  • 5g

  • 690.00CNY

  • Detail
  • TCI America

  • (B4703)  Bis(2,2,2-trifluoroethyl) Carbonate  >98.0%(GC)

  • 1513-87-7

  • 25g

  • 2,390.00CNY

  • Detail

1513-87-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name carbonic acid,2,2,2-trifluoroethanol

1.2 Other means of identification

Product number -
Other names bistrifluoroethyl carbonate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1513-87-7 SDS

1513-87-7Relevant articles and documents

Synthesis of Fluorinated Dialkyl Carbonates from Carbon Dioxide as a Carbonyl Source

Sugiyama, Masafumi,Akiyama, Midori,Nishiyama, Kohei,Okazoe, Takashi,Nozaki, Kyoko

, p. 1775 - 1784 (2020)

Fluorinated dialkyl carbonates (DACs), which serve as environmentally benign phosgene substitutes, were produced successfully from carbon dioxide either directly or indirectly. Nucleophilic addition of 2,2,2-trifluoroethanol to carbon dioxide and subsequent reaction with 2,2,2-trifluoroethyltriflate (3 a) afforded bis(2,2,2-trifluoroethyl) carbonate (1) in up to 79 % yield. Additionally, carbonate 1 was obtained through the stoichiometric reaction of 3 a and cesium carbonate. Although bis(1,1,1,3,3,3-hexafluoro-2-propyl) carbonate (4) was difficult to obtain by either of the above two methods, it could be synthesized through the transesterification of carbonate 1.

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Aldrich,P.E.,Sheppard,W.A.

, p. 11 - 15 (1964)

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Continuous method for preparing carbonate esters

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Page/Page column 16, (2021/06/09)

In one embodiment, a continuous process for preparing organic carbonate solvent of Formula (I) as described herein comprises contacting a first reactant (an alcohol) with a reactive carbonyl source (carbonyldiimidazole (CDI) or an alkylchloroformate) in the presence of a catalyst in reaction stream flowing through a continuous flow reactor at temperature 20° C. to about 160° C. and at a flow rate providing a residence time in the range of about 0.1 minute to about 24 hours; collecting a reactor effluent exiting from the continuous flow reactor; recovering a crude product from the reactor effluent; and distilling the crude product to obtain the organic carbonate compound of Formula (I). In another embodiment, the first reactant is an epoxide and the carbonyl source is carbon dioxide.

METHOD OF PRODUCING FLUORINE-CONTAINING CARBONIC ACID ESTER

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Paragraph 0077, (2020/05/02)

PROBLEM TO BE SOLVED: To provide a novel method of producing a fluorine-containing carbonic acid ester. SOLUTION: In a method of producing a fluorine-containing carbonic acid ester, a compound represented by formula (A1), a compound represented by formula (A2) and carbon dioxide are reacted in the presence of a base thereby producing a fluorine-containing carbonic acid ester represented by formula (A3), where formula (A1) is Ra1-OH, formula (A2) is Ra2-CHRa3-Lv, and formula (A3) is Ra1-O-CO-O-CHRa3-Ra2. SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT

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