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62921-35-1

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62921-35-1 Usage

Description

(12Z,14E,24Z)-5,17,19-trihydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-1,6,11-trioxo-1,2,6,7,10,11-hexahydro-2,8-(epoxytetradeca[1,11,13]trieno)[1]benzofuro[4,5-g]quinazolin-21-yl acetate is a complex organic compound with a unique fused benzofuroquinazoline ring system. It features a long, branched side chain with multiple hydroxyl and methoxy groups, as well as an epoxy group and an acetate functional group. The intricate structure of this compound suggests potential applications in pharmaceuticals or as a precursor for the synthesis of biologically active molecules. Further research and analysis are required to fully understand its properties and potential uses.

Uses

Used in Pharmaceutical Industry:
(12Z,14E,24Z)-5,17,19-trihydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-1,6,11-trioxo-1,2,6,7,10,11-hexahydro-2,8-(epoxytetradeca[1,11,13]trieno)[1]benzofuro[4,5-g]quinazolin-21-yl acetate is used as a potential pharmaceutical candidate for the development of new drugs. Its complex structure and functional groups may offer unique therapeutic properties, making it a promising molecule for further research and development.
Used in Synthesis of Biologically Active Molecules:
(12Z,14E,24Z)-5,17,19-trihydroxy-23-methoxy-2,4,12,16,18,20,22-heptamethyl-1,6,11-trioxo-1,2,6,7,10,11-hexahydro-2,8-(epoxytetradeca[1,11,13]trieno)[1]benzofuro[4,5-g]quinazolin-21-yl acetate is used as a precursor in the synthesis of biologically active molecules. Its unique structure and functional groups can be utilized to create new compounds with potential applications in various fields, such as medicine, agriculture, and materials science. Further research is needed to explore the full potential of this compound in the synthesis of novel and useful molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 62921-35-1 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 62921-35:
(7*6)+(6*2)+(5*9)+(4*2)+(3*1)+(2*3)+(1*5)=121
121 % 10 = 1
So 62921-35-1 is a valid CAS Registry Number.

62921-35-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (12S,3E,5S,13E,15Z)-7t-acetoxy-15,9c,11t-trihydroxy-5r-methoxy-12,4,6t,8c,10c,12t,16-heptamethyl-19,10-dihydro-2-oxa-1(2,8)-furo[2',3':5,6]benzo[1,2-g]quinazolina-cyclohexadecaphane-3,13,15-triene-11,6,11-trione

1.2 Other means of identification

Product number -
Other names 3-aminomethyl-O1,O4-didehydro-rifamycin cycloamidine

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:62921-35-1 SDS

62921-35-1Downstream Products

62921-35-1Relevant 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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