(14E,24E)-8-[(diethylamino)methyl]-5,6,9,17,19-pentahydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-1,11-dioxo-1,2-dihydro-2,7-(epoxypentadeca[1,11,13]trienoimino)naphtho[2,1-b]furan-21-yl acetate is a complex organic molecule with a long and intricate structure. It contains multiple functional groups including hydroxy, methoxy, and diethylamino groups, as well as a naphthofuran ring and an acetate moiety. (14E,24E)-8-[(diethylamino)methyl]-5,6,9,17,19-pentahydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-1,11-dioxo-1,2-dihydro-2,7-(epoxypentadeca[1,11,13]trienoimino)naphtho[2,1-b]furan-21-yl acetate also has several stereocenters and conjugated double bonds. The specific biological or chemical properties of (14E,24E)-8-[(diethylamino)methyl]-5,6,9,17,19-pentahydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-1,11-dioxo-1,2-dihydro-2,7-(epoxypentadeca[1,11,13]trienoimino)naphtho[2,1-b]furan-21-yl acetate are not mentioned in the name, so further information would be needed to fully understand its characteristics and potential applications. [Note: Since the provided materials do not specify any uses for (14E,24E)-8-[(diethylamino)methyl]-5,6,9,17,19-pentahydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-1,11-dioxo-1,2-dihydro-2,7-(epoxypentadeca[1,11,13]trienoimino)naphtho[2,1-b]furan-21-yl acetate, the following usage section will be omitted. If there were specific applications mentioned, they would be listed here in a similar format to the example provided for gallotannin.]
The CAS Registry Mumber 4075-41-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,7 and 5 respectively; the second part has 2 digits, 4 and 1 respectively. Calculate Digit Verification of CAS Registry Number 4075-41: (6*4)+(5*0)+(4*7)+(3*5)+(2*4)+(1*1)=76 76 % 10 = 6 So 4075-41-6 is a valid CAS Registry Number.
4075-41-6SDS
SAFETY DATA SHEETS
According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition
Version: 1.0
Creation Date: Aug 11, 2017
Revision Date: Aug 11, 2017
1.Identification
1.1 GHS Product identifier
Product name
Rifamycin PF 42
1.2 Other means of identification
Product number
-
Other names
PF-42
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).
4075-41-6Relevant academic research and scientific papers
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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