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Methyl 6-(dipropan-2-ylamino)-6-oxohexanoate is a chemical compound with the molecular formula C13H25NO3. It is a derivative of hexanoic acid, featuring a methyl ester group, a dipropan-2-ylamine substituent, and a ketone functional group. methyl 6-(dipropan-2-ylamino)-6-oxohexanoate is characterized by its potential applications in the synthesis of pharmaceuticals and other organic compounds, as well as its role as an intermediate in chemical reactions. Its structure and properties make it a versatile building block in the field of organic chemistry, particularly in the development of complex molecules with specific biological activities.

6946-67-4

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6946-67-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6946-67-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,4 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6946-67:
(6*6)+(5*9)+(4*4)+(3*6)+(2*6)+(1*7)=134
134 % 10 = 4
So 6946-67-4 is a valid CAS Registry Number.

6946-67-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 6-[di(propan-2-yl)amino]-6-oxohexanoate

1.2 Other means of identification

Product number -
Other names Adipinsaeure-diisopropylamid-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:6946-67-4 SDS

6946-67-4Downstream Products

6946-67-4Relevant academic research and scientific papers

Carboxamidation of carboxylic acids with 1-tert-butoxy-2-tert-butoxycarbonyl-1,2-dihydroisoquinoline (BBDI) without bases

Saito, Yukako,Ouchi, Hidekazu,Takahata, Hiroki

experimental part, p. 11129 - 11135 (2009/04/11)

Formation of carboxamides of a variety of carboxylic acids with the coupling reagent BBDI is described. This procedure permits a one pot and simple operation without the need of any bases and no base was?required for even use of amine hydrochlorides. In addition, an approach to BBDI-catalyzed carboxamidation is examined.

Analogues of 8-amino>-6-methoxy-4-methylquinoline as Candidate Antileishmanial Agents

LaMontagne, Maurice P.,Dagli, Dinesh,Khan, M. Sami,Blumbergs, Peter

, p. 981 - 985 (2007/10/02)

8-amino>-6-methoxy-4-methylquinoline (I) has been shown to be highly effective against Leishmania donovani in hamsters, being approximately 475 times as active as the standard meglumine antimoniate.Several nuclear and side-chain analogues of I have been prepared in an attempt to further enhance the antileishmanial activity of this class of compounds.The compounds were tested against L. donovani in the golden hamster.Although several analogues had meglumine antimoniate indexes in excess of 300, none was superior to the model compound.

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