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2-[2-(Dimethylamino)ethoxy]ethyl [3-[[[[2-[2-(dimethylamino)ethoxy]ethoxy]carbonyl]amino]methyl]-3,5,5-trimethylcyclohexyl]carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

351197-46-1

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  • 2-[2-(Dimethylamino)ethoxy]ethyl [3-[[[[2-[2-(dimethylamino)ethoxy]ethoxy]carbonyl]amino]methyl]-3,5,5-trimethylcyclohexyl]carbamate

    Cas No: 351197-46-1

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351197-46-1 Usage

Molecular structure

The compound has a long and complex molecular structure, consisting of several functional groups such as ethoxy, carbamate, and dimethylamino groups.

Functional groups

The main functional groups present in the compound are ethoxy (-O-CH2-CH3), carbamate (-O-CO-NH2), and dimethylamino (-N(CH3)2).

Ethoxy group

This group is formed by an ether bond between an oxygen atom and an ethyl group (-CH2-CH3). It contributes to the compound's solubility and reactivity with other molecules.

Carbamate group

The carbamate group is a functional group that consists of a carbonyl group (C=O) and an amino group (-NH2) bonded to the same carbon atom. It is often found in pharmaceuticals and pesticides due to its ability to react with biological targets.

Dimethylamino group

This group consists of an amino group (-NH2) with two methyl groups (-CH3) attached to it. It is a basic functional group that can participate in hydrogen bonding and other interactions with other molecules.

Cyclohexyl ring

The compound contains a cyclohexyl ring, which is a six-membered carbon ring with single bonds. This ring structure contributes to the compound's stability and rigidity.

Trimethyl substitution

The cyclohexyl ring in the compound is substituted with three methyl groups (-CH3), which can influence the compound's lipophilicity and solubility.

Potential applications

The compound may have potential applications in pharmaceuticals, organic synthesis, and material science due to its complex structure and various functional groups.

Biological activity

The compound's structure suggests that it may have biological activity, but further research and testing would be needed to fully understand its potential uses.

Building block for complex chemicals

The compound could also serve as a building block for the synthesis of more complex chemicals, given its diverse functional groups and structural features.

Check Digit Verification of cas no

The CAS Registry Mumber 351197-46-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,1,1,9 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 351197-46:
(8*3)+(7*5)+(6*1)+(5*1)+(4*9)+(3*7)+(2*4)+(1*6)=141
141 % 10 = 1
So 351197-46-1 is a valid CAS Registry Number.

351197-46-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-[2-(dimethylamino)ethoxy]ethyl N-[3-[[2-[2-(dimethylamino)ethoxy]ethoxycarbonylamino]methyl]-3,5,5-trimethylcyclohexyl]carbamate

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:351197-46-1 SDS

351197-46-1Downstream Products

351197-46-1Relevant articles and documents

METHOD FOR PRODUCING TRIARYLORGANOBORATES

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Paragraph 0266, (2019/09/06)

The invention relates to a process for preparing triaryl organoborates proceeding from organoboronic esters in the presence of an n-valent cation 1/n Kn+, comprising the anhydrous workup of the reaction mixture and the use of the triaryl organoborates obtained as co-initiator in photopolymer formulations, holographic media and holograms.

PROCESS FOR THE PRODUCTION OF TRIARYL ORGANOBORATES

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Paragraph 0131-0132, (2019/09/20)

The invention relates to a process for preparing triaryl organoborates proceeding from alkyl or cycloalkyl boronates in the presence of an n-valent cation 1/n Kn+ and to the use of these substances as co-initiator in photopolymer formulations.

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