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62921-38-4

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62921-38-4 Usage

General Description

The chemical "(12Z,14E,24Z)-5,17,19-trihydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-1,6,11-trioxo-1,2,6,11-tetrahydro-2,8-(epoxytetradeca[1,11,13]trieno)[1]benzofuro[4,5-g]quinazolin-21-yl acetate" is a complex organic compound with a long and detailed molecular structure. It contains multiple functional groups, including hydroxyl, methoxy, and acetate groups, as well as a unique benzofuroquinazolin-21-yl moiety. The compound also features a large and intricate ring system, with several fused rings and an epoxy group. This chemical likely possesses diverse biological activities and pharmaceutical potential due to its complex structure and the presence of multiple functional groups.

Check Digit Verification of cas no

The CAS Registry Mumber 62921-38-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,2 and 1 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 62921-38:
(7*6)+(6*2)+(5*9)+(4*2)+(3*1)+(2*3)+(1*8)=124
124 % 10 = 4
So 62921-38-4 is a valid CAS Registry Number.

62921-38-4Downstream Products

62921-38-4Relevant articles and documents

3-N-substituted aminomethyl derivatives of rifamycin SV. A convenient method of synthesis, cyclization of certain derivatives, and anticellular and antiviral activities of several derivatives

McCarthy,Moore,Wysong,Aldrich

, p. 1272 - 1276 (2007/10/21)

A new synthesis of Mannich bases of rifamycin SV using the Borch procedure with rifaldehyde is described. This new synthesis offers two advantages over the previously published method. It provides a route to monoalkyl-aminomethylrifamycins (1e-h) and to unsubstituted aminomethylrifamycins that were not accessible by the old procedure. The new method also offers a preparative route to Mannich bases 1a and 1b which were needed in multigram quantities for biological testing. In addition, the cyclization of certain of the monoalkylaminomethylrifamycins to the novel N,15 didehydro 15 deoxo 3,15 epi[methano(alkylimino)]rifamycin SV derivatives is described. The anticellular and antiviral effects of representatives of both series of compounds against cultured mouse cells and murine oncornavirus are discussed.

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