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93839-70-4

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93839-70-4 Usage

Description

4-[(2-aminobenzyl)amino]cyclohexan-1-ol is a chemical compound with the molecular formula C13H20N2O. It is an amino alcohol derivative that belongs to the class of cyclohexanes. 4-[(2-aminobenzyl)amino]cyclohexan-1-ol consists of a cyclohexane ring with an amino group and a benzyl group attached to it. The presence of an alcohol group in the molecule adds to its reactivity and potential applications. It may have uses in organic synthesis, pharmaceuticals, or as a building block for other chemical compounds. Further research and analysis are required to fully understand its properties and potential uses.

Uses

Used in Organic Synthesis:
4-[(2-aminobenzyl)amino]cyclohexan-1-ol is used as a building block for the synthesis of other chemical compounds. Its unique structure and functional groups make it a versatile component in the creation of various organic molecules.
Used in Pharmaceutical Industry:
4-[(2-aminobenzyl)amino]cyclohexan-1-ol is used as an intermediate in the development of pharmaceuticals. Its reactivity and structural features may contribute to the design and synthesis of new drugs with potential therapeutic applications.
Used in Chemical Research:
4-[(2-aminobenzyl)amino]cyclohexan-1-ol is used as a subject of study in chemical research. Its properties and potential uses are being investigated to gain a deeper understanding of its behavior and to explore its possible applications in various fields.

Check Digit Verification of cas no

The CAS Registry Mumber 93839-70-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,8,3 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 93839-70:
(7*9)+(6*3)+(5*8)+(4*3)+(3*9)+(2*7)+(1*0)=174
174 % 10 = 4
So 93839-70-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H20N2O/c14-13-4-2-1-3-10(13)9-15-11-5-7-12(16)8-6-11/h1-4,11-12,15-16H,5-9,14H2

93839-70-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(2-aminophenyl)methylamino]cyclohexan-1-ol

1.2 Other means of identification

Product number -
Other names 4-[(2-AMINOBENZYL)AMINO]CYCLOHEXAN-1-OL

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:93839-70-4 SDS

93839-70-4Downstream Products

93839-70-4Relevant articles and documents

Ambroxol hydrochloride production process

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Paragraph 0034-0037, (2021/09/29)

The invention relates to an ambroxol hydrochloride production process which comprises the following steps: dropwise adding o-nitrobenzyl bromide into trans-4-aminocyclohexanol to carry out condensation reaction to obtain an N-(o-nitrophenyl)-trans-4-aminocyclohexanol chloroform reaction solution, adding hydrochloric acid, and separating the solution to obtain an N-(o-nitrophenyl)-trans-4-aminocyclohexanol hydrochloride aqueous solution; adding toluene into a hydrochloride aqueous solution to obtain an N-(o-aminophenyl)-trans-4-aminocyclohexanol toluene reaction solution; adding sulfuric acid into the toluene reaction solution to obtain an N-(o-aminophenyl)-trans-4-aminocyclohexanol sulfuric acid reaction solution; and carrying out bromination reaction in a sulfuric acid reaction solution, filtering out 2-amino-3,5-dibromo-N-(trans-4-hydroxycyclohexyl)benzylamine salt, and dissolving, purifying and refining the benzylamine salt to obtain ambroxol hydrochloride. According to the preparation method, o-nitrobenzyl bromide is adopted as a starting raw material and is subjected to condensation with trans-4-aminocyclohexanol, reduction, bromination and salification refining, the ambroxol hydrochloride is obtained, the total yield reaches 85% or above, the raw materials are easy to obtain, operation is convenient and fast, and the raw material cost can be saved by 40%-50%.

Synthesis of the metabolites from Bisolvon

Keck

, p. 107 - 111 (2007/10/06)

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