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2-Propanol,1,1'-[(p-methoxyphenyl)imino]bis[3-chloro- (7CI,8CI) is a complex organic compound with the chemical formula C16H18Cl2NO2. It is a derivative of 2-propanol, featuring a unique structure that includes a p-methoxyphenyl group connected to two 3-chloro-2-propanol molecules through an imino linkage. 2-Propanol,1,1'-[(p-methoxyphenyl)imino]bis[3-chloro- (7CI,8CI) is characterized by its two chlorine atoms and a methoxy group, which contribute to its chemical properties. It is important to note that the compound's specific applications, safety considerations, and synthesis methods are not detailed in this summary, but it serves as a brief overview of its chemical composition and structure.

4643-49-6

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4643-49-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4643-49-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,4 and 3 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4643-49:
(6*4)+(5*6)+(4*4)+(3*3)+(2*4)+(1*9)=96
96 % 10 = 6
So 4643-49-6 is a valid CAS Registry Number.

4643-49-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-3-(N-(3-chloro-2-hydroxypropyl)-4-methoxyanilino)propan-2-ol

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

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More Details:4643-49-6 SDS

4643-49-6Relevant academic research and scientific papers

PREPARATION OF SOME DERIVATIVES OF BENZOQUINOLIZINE

Silhankova, Alexandra,Trska, Petr,Vlkova, Daniela,Ferles, Miloslav

, p. 1048 - 1056 (2007/10/02)

Reaction of 1,2,3,4-tetrahydroquinoline with 1-chloro-2,3-epoxypropane afforded 1-(3-chloro-2-hydroxypropyl)-1,2,3,4-tetrahydroquinoline (IIb) which was thermolabile and on heating in vacuo was converted into 2,3,6,7-tetrahydro-1H,5H-benzoquinolizin-2-ol (Ib).This compound reacted with acetic anhydride and p-toluenesulfonyl chloride to give 2-acetoxy-2,3,6,7-tetrahydro-1H,5H-benzoquinolizine (Ic) and 2-(p-toluenesulfonyloxy)-2,3,6,7-tetrahydro-1H,5H-benzoquinolizine (Id), respectively.N,N-Bis(3-chloro-2-hydroxypropyl)aniline (IIIb) on heating gave a mixture of cis- and trans-2,3,6,7-tetrahydro-1H,5H-benzoquinolizine-2,6-diols (Ie).The corresponding 4-methoxyaniline derivative afforded analogously a mixture of cis- and trans-9-methoxy-2,3,6,7-tetrahydro-1H,5H-benzoquinolizine-2,6-diols (If).Dehydration with potassium hydroxide converted the diols Ie into 1H,7H-benzoquinolizine (VIa), the diols If into 9-methoxy-1H,7H-benzoquinolizine (VIb).Treatment of Ib with phosphorus pentoxide led to 2,3,6,7-tetrahydro-1H,5H-benzoquinolizine (julolidine, Ia).

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