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Morpholine, 4-(difluoroacetyl)- (8CI,9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27074-57-3

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27074-57-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27074-57-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,0,7 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 27074-57:
(7*2)+(6*7)+(5*0)+(4*7)+(3*4)+(2*5)+(1*7)=113
113 % 10 = 3
So 27074-57-3 is a valid CAS Registry Number.

27074-57-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,2-difluoro-1-morpholino-ethanone

1.2 Other means of identification

Product number -
Other names 2',2'-Difluoro-1'-methylstyrene

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:27074-57-3 SDS

27074-57-3Relevant academic research and scientific papers

Ring opening reactions of cyclic sulfamidates. Synthesis of β-fluoroaryl alanines and derivatives of 4,4-difluoroglutamic acid

Bolek, Sylwia,Ignatowska, Jolanta

, p. 13 - 21 (2019)

Ring opening reactions of 1 with copper complex formed between Cu, TMEDA and BrCF2CO2Et lead to optically active 4,4-difluoroglutamic acid derivatives 11a-d in moderate yields. Reaction of cyclic sulfamidates 1 with fluoro substituted arylmagnesium chlorides proceed via copper catalyzed 1,4-addition of Grignard reagent to dehydroalanine 2, formed in situ. Fluorinated organoznic derivatives were unreactive towards 1 regardless of the reaction conditions; instead product of reaction of 1 with DMF was isolated.

Preparation method of 2, 2-difluoroacetamide derivative

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Paragraph 0036-0038, (2020/05/05)

The invention discloses a preparation method of a 2,2-difluoroacetamide derivative. The preparation method is characterized in that a 2,2-dichloroacetamide derivative is subjected to potassium fluoride fluorination under the action of a catalyst N-[di(diethylamino)methylene]-N-ethyl-ethane ammonium halide and an organic solvent to generate the 2,2-difluoroacetamide derivative. The preparation method of the 2,2-difluoroacetamide derivative disclosed by the invention is simple in production process and high in yield, the catalyst can be repeatedly used, the production cost can be effectively reduced, and the preparation method is suitable for large-scale industrial production.

Substituted Nitrogen Heterocycles and Synthesis and Uses Thereof

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Page/Page column 27-28, (2009/10/06)

The invention relates to a nitrogen heterocycle compound of formula 1: Also disclosed are a method of synthesizing the compound and use of the compound for treating various diseases and conditions.

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