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24653-40-5

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24653-40-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24653-40-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,6,5 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 24653-40:
(7*2)+(6*4)+(5*6)+(4*5)+(3*3)+(2*4)+(1*0)=105
105 % 10 = 5
So 24653-40-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H17NO3/c1-4-12(5-2)8-9-6-7-10(15-9)11(13)14-3/h6-7H,4-5,8H2,1-3H3

24653-40-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 5-(diethylaminomethyl)furan-2-carboxylate

1.2 Other means of identification

Product number -
Other names 5-Diaethylaminomethyl-furan-2-carbonsaeure-methylester

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:24653-40-5 SDS

24653-40-5Relevant articles and documents

Antimuscarinic agents: Furan analogs of benzilate esters

Stubbins,Hudgins,Murphy

, p. 534 - 537 (2007/10/02)

The methiodide and ethiodide salts of 5-(dimethylaminomethyl)- and 5-(diethylaminomethyl)-α,α-diphenylfurfuryl alcohol were prepared. These compounds may be considered as furan analogs of dialkylaminoethyl benzilate alkiodides. The pA2 values of these compounds as antagonists of acetylcholine were determined on rat jejunum preparation. All four compounds were significantly less potent than the analogous ester antimuscarinic lachesine. The furan ring cannot be substituted for the ester moiety of typical antimuscarinics. Possible modes of binding by antagonists to the receptor proposed previously are considered that might account for this less-than-expected antimuscarinic activity.

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