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55305-15-2

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55305-15-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55305-15-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,3,0 and 5 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55305-15:
(7*5)+(6*5)+(5*3)+(4*0)+(3*5)+(2*1)+(1*5)=102
102 % 10 = 2
So 55305-15-2 is a valid CAS Registry Number.

55305-15-2Downstream Products

55305-15-2Relevant articles and documents

New method for the synthesis of pyrromethanes

Okada, Kunisuke,Saburi, Kiyoshi,Nomura, Keishi,Tanino, Hideo

, p. 2127 - 2131 (2007/10/03)

Coupling reaction of 2-mercaptobenzothiazolylmethylpyrrole with α-free pyrrole in the presence of silver(I) triflate proceeds smoothly at room temperature to give a pyrromethane in excellent yield. The azafulvenium ion, an active form that reacts with α-f

Reactions on solid supports part II: a convenient method for synthesis of pyrromethanes using a montmorillonite clay as catalyst

Jackson, Anthony H.,Pandey, Ravindra K.,Nagaraja Rao,Roberts, Edward

, p. 793 - 796 (2007/10/02)

α-Acetoxymethylpyrroles couple with α-free pyrroles in presence of Montmorillonite clay to form unsymmetrical pyrromethanes in excellent yields. Symmetrical pyrromethanes were also prepared in a similar manner by clay catalysed self-condensation of α-acet

SYNTHESIS OF UROPORPHYRIN-III, AND RELATED HEPTA- AND PENTA-CARBOXYLIC PORPHYRINS BY MODIFICATIONS OF THE MACDONALD METHOD

Chakrabarty, M.,Ali, S. A.,Philip, G.,Jackson, A. H.

, p. 1199 - 1204 (2007/10/02)

A modification of the MacDonald route has been developed in which all four pyrrole units of uroporphyrin-III have been derived from the same conveniently prepared starting pyrrole.Related hepta- and penta-carboxylic porphyrins have also been synthesised by condensation of appropriate α-formyl pyrromethane-α'-carboxylic acids; in each case other porphyrins with different numbers of acidic side-chains were also produced but the desired products were easily separated (as their methyl esters) by h.p.l.c.

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