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2,3,9,10-tetramethoxy-13-methyl-5,6-dihydroisoquino[3,2-a]isoquinolinium iodide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37553-95-0

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37553-95-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37553-95-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,5,5 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 37553-95:
(7*3)+(6*7)+(5*5)+(4*5)+(3*3)+(2*9)+(1*5)=140
140 % 10 = 0
So 37553-95-0 is a valid CAS Registry Number.

37553-95-0SDS

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 2,3,9,10-tetramethoxy-13-methyl-5,6-dihydroisoquinolino[2,1-b]isoquinolin-7-ium,iodide

1.2 Other means of identification

Product number -
Other names Dibenzo(a,g)quinolizinium,5,6-dihydro-2,3,9,10-tetramethoxy-13-methyl-,iodide

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:37553-95-0 SDS

37553-95-0Downstream Products

37553-95-0Relevant academic research and scientific papers

A urethane-based paint film composition

-

, (2007/10/09)

PROBLEM TO BE SOLVED: To provide a urethane-base coating-film waterproof material composition odorless and excellent in mixability, curability and finishing touches, low in viscosity and hard to foam. SOLUTION: This urethane-base coating-film waterproof material composition comprises a urethane prepolymer, a curing agent, and 2,2,4-trimethyl-1,3-pentane diol diisobutyrate, wherein the 2,2,4-trimethyl-1,3-pentane diol diisobutyrate is contained in an amount of 1-15 pts. by mass to 100 pts. by mass of components other than the 2,2,4-trimethyl-1,3-pentane diol diisobutyrate. COPYRIGHT: (C)2006,JPOandNCIPI

A regiospecific synthesis of protoberberine alkaloids

Kiparissides, Zinovia,Fichtner, Robert H.,Poplawski, Janusz,Nalliah, Bala C.,MacLean, David B.

, p. 2770 - 2779 (2007/10/02)

The protoberberine skeleton has been prepared in two steps from N-benzyl-3,4-dihydroisoquinolinium salts.Treatment of the salts with the anion of methyl methylthiomethylsulfoxide yields mixtures of diastereomeric adducts that cyclize on heating with concentrated hydrochloric acid to dihydroprotoberberines.The latter compounds may be reduced to their tetrahydro analogues with sodium borohydride, oxidized to protoberberinium salts with iodine, or converted to 13-methyltetrahydroprotoberberines by treatment with formaldehyde according to an established procedure.The method has been applied successfully to the synthesis of (+/-)-tetrahydropalmatine, palmatine iodide, (+/-)-xylopinine, (+/-)-sinactine, and (+/-)-corydaline.N-Benzylisoquinolinium salts may be used in place of their dihydro analogues as starting materials in this synthesis, thereby extending the range of substitution patterns potentially available.

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