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5564-73-8

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5564-73-8 Usage

General Description

1-(DIMETHOXYMETHYL)PYRROLIDINE is a chemical compound with the molecular formula C8H17NO2. It is a derivative of pyrrolidine and contains two methoxy (CH3O) functional groups attached to a central pyrrolidine ring. It is commonly used as a building block in the synthesis of various pharmaceuticals, agrochemicals, and fine chemicals. The compound has been studied for its potential antimicrobial, antifungal, and anti-inflammatory properties. Due to its versatile nature and reactivity, 1-(DIMETHOXYMETHYL)PYRROLIDINE is used in various chemical reactions and processes in the pharmaceutical and chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 5564-73-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,6 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5564-73:
(6*5)+(5*5)+(4*6)+(3*4)+(2*7)+(1*3)=108
108 % 10 = 8
So 5564-73-8 is a valid CAS Registry Number.

5564-73-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(DIMETHOXYMETHYL)PYRROLIDINE

1.2 Other means of identification

Product number -
Other names N-(dimethoxymethyl)pyrrolidine

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:5564-73-8 SDS

5564-73-8Relevant articles and documents

N-6-dialkylformamidine-2'-deoxyadenosine phosphoramidites in oligodeoxynucleotide synthesis. Rapid deprotection of oligodeoxynucleotides

Theisen,McCollum,Andrus

, p. 1033 - 1046 (1993)

-

Copper-catalyzed coupling reaction of c-ome bonds adjacent to a nitrogen atom with terminal alkynes

Yao, Bangben,Zhang, Yuhong,Li, Yong

supporting information; experimental part, p. 4554 - 4561 (2010/09/10)

(Figure presented) The cross coupling of the C-OMe bond adjacent to a nitrogen atom in dialkoxy-N,N-dialkylmethanamines with terminal alkynes was efficiently approached in the presence of copper catalyst under mild conditions to give 3-amino-1,4-diynes in good yields. The reaction is promoted by phosphine ligands and the chemistry provides a simple and efficient route to 3-amino-1,4-diynes. Importantly, the Michael addition occurred with as-prepared 3-amino-1,4-diynes to give the useful Michael-adducts containing tert-alkylamines in a very convenient way. Further studies revealed that (E)-1,5-diarylpent-1-en-4-yn-3-one was formed through the rearrangement by using the neutral alumina column, and the corresponding imine 2-(1,5-diphenylpent-2- en-4-ynylideneamino)ethanol was obtained in the presence of AgOTf.

A spectroscopic investigation of donor-acceptor-substituted heptalenes

Ott, Philipp,Hansen, Hans-Juergen

, p. 2670 - 2692 (2007/10/03)

It is shown that the heptalene-4,5-dicarboxylates 5 react with their Me group at C(1) with N,N-dimethylformamide dimethyl acetal or other acetals of this type in N,N-dimethylformamide (DMF) to give the corresponding 1-[(E)-2-(N,N-dialkylamino)ethenyl]-sub

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