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56879-47-1

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56879-47-1 Usage

General Description

4-(Aminomethyl)-N-hydroxybenzimidamide is a chemical compound with the molecular formula C9H11N3O2. It is a derivative of benzimidazole and contains both an aminomethyl and a hydroxy group. 4-(AMINOMETHYL)-N-HYDROXYBENZIMIDAMIDE has the potential to act as a reactive intermediate in various chemical reactions, and its unique structure and properties make it a valuable building block for the synthesis of other organic compounds. It is also known for its potential biological activity, and it has been studied for its possible role as a therapeutic agent in various medical applications. Overall, 4-(Aminomethyl)-N-hydroxybenzimidamide is a versatile and interesting chemical with potential applications in both chemistry and biology.

Check Digit Verification of cas no

The CAS Registry Mumber 56879-47-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,8,7 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 56879-47:
(7*5)+(6*6)+(5*8)+(4*7)+(3*9)+(2*4)+(1*7)=181
181 % 10 = 1
So 56879-47-1 is a valid CAS Registry Number.

56879-47-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(AMINOMETHYL)-N-HYDROXYBENZIMIDAMIDE

1.2 Other means of identification

Product number -
Other names -

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:56879-47-1 SDS

56879-47-1Downstream Products

56879-47-1Relevant articles and documents

Modular Chemoenzymatic Synthesis of GE81112 B1 and Related Analogues Enables Elucidation of Its Key Pharmacophores

Zwick, Christian R.,Sosa, Max B.,Renata, Hans

supporting information, p. 1673 - 1679 (2021/01/25)

The GE81112 complex has garnered much interest due to its broad antimicrobial properties and unique ability to inhibit bacterial translation initiation. Herein we report the use of a chemoenzymatic strategy to complete the first total synthesis of GE81112 B1. By pairing iron and α-ketoglutarate dependent hydroxylases found in GE81112 biosynthesis with traditional synthetic methodology, we were able to access the natural product in 11 steps (longest linear sequence). Following this strategy, 10 GE81112 B1 analogues were synthesized, allowing for identification of its key pharmacophores. A key feature of our medicinal chemistry effort is the incorporation of additional biocatalytic hydroxylations in modular analogue synthesis to rapidly enable exploration of relevant chemical space.

Furan-Derived Chiral Bicycloaziridino Lactone Synthon: Collective Syntheses of Oseltamivir Phosphate (Tamiflu), (S)-Pipecolic acid and its 3-Hydroxy Derivatives

Chavan, Subhash P.,Gonnade, Rajesh G.,Kadam, Appasaheb L.,Shinde, Shrikrishna S.

, (2020/02/05)

A unified synthetic strategy for oseltamivir phosphate (tamiflu), (S)-pipecolic acid, and its 3-hydroxy derivatives from furan derived common chiral bicycloaziridino lactone synthon is described here. Key features are the short (4-steps), enantiopure, and decagram-scale synthesis of common chiral synthon from furan and its first-ever application in the total synthesis of biologically active compounds by taking the advantages of high functionalization ability of chiral synthon.

Synthesis of (+)-L-733,060, (+)-CP-99,994 and (2S,3R)-3-hydroxypipecolic acid: Application of an organocatalytic direct vinylogous aldol reaction

Pansare, Sunil V.,Paul, Eldho K.

experimental part, p. 2119 - 2125 (2012/04/17)

The γ-butenolide obtained from an organocatalyzed, direct vinylogous aldol reaction of γ-crotonolactone and benzaldehyde serves as the key starting material in the expedient synthesis of a 3-hydroxy-2-phenyl piperidine intermediate which is converted to the target 2,3-disubstituted piperidines.

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