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62206-16-0

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62206-16-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62206-16-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,0 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 62206-16:
(7*6)+(6*2)+(5*2)+(4*0)+(3*6)+(2*1)+(1*6)=90
90 % 10 = 0
So 62206-16-0 is a valid CAS Registry Number.

62206-16-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,7-dimethoxy-1-(5-chloro-2-aminophenyl)-1,2,3,4-tetrahydroisoquinoline

1.2 Other means of identification

Product number -
Other names 4-chloro-2-(6,7-dimethoxy-1,2,3,4-tetrahydro-isoquinolin-1-yl)-aniline

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:62206-16-0 SDS

62206-16-0Downstream Products

62206-16-0Relevant articles and documents

Synthesis and?antitumor activity of?cis-dichloroplatinum(II) complexes of?1-(2-aminophenyl)-1,2,3,4-tetrahydroisoquinolines

Kuo, Chen-Yuan,Wu, Ming-Jung,Kuo, Yao-Haur

, p. 940 - 949 (2007/10/03)

Fifteen cis-dichloroplatinum complexes (5a-5o) were synthesized by treatment of 1-(2-aminophenyl)-1,2,3,4-THIQs (4a-4o) with K2PtCl4. The antitumor activity of these compounds was examined against four different human tumor cell lines. Their structure-activity relationships for antitumor activity are reported. All of these compounds exhibited activity against MCF-7 cell line and showed good activity against WiDr cell line except 5c and 5f. On the other hand, compounds 5j and 5o are more active than the other compounds against Hepa59T/VGH cell line. The electron-donating group at the 6-position of isoquinoline ring seems to decrease the antitumor activity and the chloro substituent at the C-4 position of the aniline ring shown the highest potency. The "trans influence" dominates the control of the stability of [1-(2-aminophenyl)-1,2,3,4-THIQ]dichloroplatinums(II).

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