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1-Propanol, 2,2-dimethyl-, 2-aminobenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67836-91-3

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67836-91-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67836-91-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,8,3 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 67836-91:
(7*6)+(6*7)+(5*8)+(4*3)+(3*6)+(2*9)+(1*1)=173
173 % 10 = 3
So 67836-91-3 is a valid CAS Registry Number.

67836-91-3Relevant academic research and scientific papers

Synthesis of simple analogues of methyllycaconitine - An efficient method for the preparation of the N-substituted anthranilate pharmacophore

Barker, David,Brimble, Margaret A.,McLeod, Malcolm D.

, p. 5953 - 5963 (2007/10/03)

The synthesis of several A and AE ring analogues of the alkaloid methyllycaconitine is reported. The key 2-(2″-methylsuccinimido)benzoate ester pharmacophore is introduced using an efficient two step procedure. Esterification of the alcohol precursors with N-(trifluoroacetyl)anthranilic acid under Steglich conditions followed by sodium borohydride mediated cleavage of the trifluoroacetyl group affords the anthranilate esters. Subsequent fusion with methylsuccinic anhydride affords the N-substituted anthranilate derivatives containing the key pharmacophore present in a range of commonly occurring Delphinium and Aconitum alkaloids.

A high yielding synthesis of anthranilate esters from sterically hindered alcohols

Barker, David,McLeod, Malcolm D.,Brimble, Margaret A.,Savage, G. Paul

, p. 1785 - 1788 (2007/10/03)

A high yielding and operationally simple synthesis of anthranilate esters derived from primary, secondary and tertiary alcohols is reported. Esterification of the alcohol with N-(trifluoroacetyl)anthranilic acid under Steglich conditions, followed by sodium borohydride mediated cleavage of the trifluoroacetyl group affords the anthranilate ester. This new method has application in the synthesis of the ester sidechains of the commonly occurring Delphinium and Aconitum alkaloids and their analogues.

Acylation of lycoctonine: Semi-synthesis of inuline, delsemine analogues and methyllycaconitine

Blagbrough, Ian S.,Coates, Philippa A.,Hardick, David J.,Lewis, Terence,Rowan, Michael G.,Wonnacott, Susan,Potter, Barry V. L.

, p. 8705 - 8708 (2007/10/02)

Lycoctonine has been acylated to afford sequentially inuline, delsemine analogues and methyllycaconitine using isatoic anhydride followed by S-(-)-methylsuccinic anhydride. This protocol is a rapid, facile method for the regiospecific introduction of the

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