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3-methoxy-N,N-bis(3-methylbut-2-enyl)aniline hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1073190-52-9

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1073190-52-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1073190-52-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,3,1,9 and 0 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1073190-52:
(9*1)+(8*0)+(7*7)+(6*3)+(5*1)+(4*9)+(3*0)+(2*5)+(1*2)=129
129 % 10 = 9
So 1073190-52-9 is a valid CAS Registry Number.

1073190-52-9SDS

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 3-methoxy-N,N-bis(3-methylbut-2-enyl)aniline hydrochloride

1.2 Other means of identification

Product number -
Other names 3-methoxy-N,N-bis(3-methylbut-2-ene)aniline hydrochloride

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:1073190-52-9 SDS

1073190-52-9Relevant academic research and scientific papers

3,6-DISUBSTITUTED XANTHYLIUM SALTS

-

Page/Page column 87, (2010/07/02)

This invention pertains generally to processes, uses, methods and materials utilising particular xanthylium compounds, including compounds of formula (I) and (II), as further defined herein. These compounds are useful as drugs, for example, in the treatment of tauopathies, such as Alzheimer's disease.

Synthesis of 5- and 6-carboxy-x-rhodamines

Uddin, Md Jashim,Marnett, Lawrence J.

supporting information; experimental part, p. 4799 - 4801 (2009/05/31)

(Equation Presented) An efficient route is reported to 5- and 6-carboxy-X-rhodamines (compounds 1 and 2) that contain multiple n-propylene or y,y-dimethylpropylene groups bridging terminal nitrogen atoms and the central xanthene core. Gram quantities of these dyes are synthesized from inexpensive starting materials. The isolated products are activated by selective transformation of the carboxylic acid group into N-hydroxysuccinimidyl esters in situ and then conjugated with an amino group of a molecule of interest.

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