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4,6-Di-1H-imidazol-1-yl-N,N-dimethyl-1,3,5-triazin-2-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

153429-75-5

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153429-75-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 153429-75-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,4,2 and 9 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 153429-75:
(8*1)+(7*5)+(6*3)+(5*4)+(4*2)+(3*9)+(2*7)+(1*5)=135
135 % 10 = 5
So 153429-75-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H12N8/c1-17(2)9-14-10(18-5-3-12-7-18)16-11(15-9)19-6-4-13-8-19/h3-8H,1-2H3

153429-75-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4,6-di(imidazol-1-yl)-N,N-dimethyl-1,3,5-triazin-2-amine

1.2 Other means of identification

Product number -
Other names 4,6-Di-1H-imidazol-1-yl-N,N-dimethyl-1,3,5-triazin-2-amine

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:153429-75-5 SDS

153429-75-5Downstream Products

153429-75-5Relevant academic research and scientific papers

Synthesis and aromatase-inhibitory activity of imidazolyl-1,3,5-triazine derivatives

Matsuno, Toshiyuki,Kato, Masanobu,Tsuchida, Yoshio,Takahashi, Masayuki,Yaguchi, Sin-Ichi,Terada, Sumio

, p. 291 - 296 (2007/10/03)

Triamino-substituted 1,3,5-triazine derivatives were synthesized and tested for inhibitory activities against the aromatase of human placental microsomes and the cytochrome P450 side chain cleavage of cholesterol (P450(SCC)) of pig adrenal mitochondria. The compounds having imidazolyl and tertiary amino groups as substituents in the 1,3,5-triazine ring showed significant aromatase-inhibitory activity. Among them, compounds 17, 23, 26, 27 and 28 were more active than the reference compound, CGS 16949A. The inhibitory activities of these compounds against P450(SCC) were much weaker than their aromatase-inhibitory activities. These compounds may be regarded as selective aromatase inhibitors.

S-triazine derivative and remedy for estrogen-dependent disease containing said derivative as effective component

-

, (2008/06/13)

s-Triazine (1,3,5-triazine) is chemically modified to obtain s-triazine derivative effective for prevention and treatment of estrogen-dependent diseases.

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