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23590-03-6

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23590-03-6 Usage

General Description

2-(dibutylamino)acetic acid is a chemical compound with the molecular formula C12H25NO2. It is a derivatives of acetic acid, with a dibutylamino group (C8H17N) attached to the carbon atom. 2-(dibutylamino)acetic acid is commonly used as a pharmaceutical intermediate and in the synthesis of other organic compounds. It has applications in the production of drugs, agrochemicals, and materials. 2-(dibutylamino)acetic acid is considered to be a low-to-moderate hazard chemical and should be handled with proper safety precautions.

Check Digit Verification of cas no

The CAS Registry Mumber 23590-03-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,5,9 and 0 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 23590-03:
(7*2)+(6*3)+(5*5)+(4*9)+(3*0)+(2*0)+(1*3)=96
96 % 10 = 6
So 23590-03-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H21NO2/c1-3-5-7-11(8-6-4-2)9-10(12)13/h3-9H2,1-2H3,(H,12,13)

23590-03-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(dibutylamino)acetic acid

1.2 Other means of identification

Product number -
Other names Glycine,N,N-dibutyl

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:23590-03-6 SDS

23590-03-6Relevant articles and documents

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Nash,C.P.,Schaefer,W.P.

, p. 1319 - 1324 (1969)

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An ionic compound, and an electrolyte solution and a secondary battery comprising an ionic compound

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Paragraph 0108; 0113; 0115; 0126; 0129-0130, (2020/04/17)

An electrolyte for a secondary, battery and Si an electrolytic solution for a secondary battery and 1 a 2 secondary battery comprising the same are provided to improve the stability of a secondary battery by using an ionic compound having a structure represented by the following Chemical Formula I, No.No. STR84No.No. wherein X is an ionic compound having a structure represented by Structural Formula (I). No.No. STR84No.No. The compound of formula ( Claim The compound of formula ( Claim (by machine translation)

SULFONYLIMIDE SALT AND METHOD FOR PRODUCING THE SAME

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Page/Page column 12, (2011/02/26)

The present invention provides a method for producing fluorosulfonylimides more safely, rapidly and efficiently, which enables suppression of production of by-products, and fluorosulfonylimides. The method for producing a fluorosulfonylimide salt of the present invention includes a step of reacting a fluoride compound containing at least one element selected from the group consisting of elements of Group 11 to Group 15 and Period 4 to Period 6 (excluding arsenic and antimony) with a compound represented by the following general formula (I) to give a fluorosulfonylimide salt represented by the general formula (II): wherein R1 denotes at least one element selected from the group consisting of elements of Group 11 to Group 15 and Period 4 to Period 6 (excluding arsenic and antimony); R3 denotes fluorine, chlorine or a fluorinated alkyl group having 1 to 6 carbon atoms; R4 denotes fluorine or a fluorinated alkyl group having 1 to 6 carbon atoms; and m denotes an integer of 2 or 3.

Diphenylboron Chelates of α-(Dialkylamino)carboxylic Acids and their N-Oxides

Kliegel, Wolfgang,Graumann, Juergen

, p. 950 - 961 (2007/10/02)

α-(Dialkylamino)carboxylic acids and their N-oxides react with oxybis(diphenylborane) or similar diphenylborane derivatives to give five- or six-membered diphenylboron chelate rings, respectively, the structure of which is supported by spectroscopic evidence.

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