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Benzamide, N-(6-amino-1,2,3,4-tetrahydro-2,4-dioxo-1,3-dipropyl-5-pyrimidinyl)-3,5-dichloro-2-[(trifluoroacetyl)amino]- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

154623-75-3

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154623-75-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 154623-75-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,4,6,2 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 154623-75:
(8*1)+(7*5)+(6*4)+(5*6)+(4*2)+(3*3)+(2*7)+(1*5)=133
133 % 10 = 3
So 154623-75-3 is a valid CAS Registry Number.

154623-75-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-amino-2,6-dioxo-1,3-dipropylpyrimidin-5-yl)-3,5-dichloro-2-[(2,2,2-trifluoroacetyl)amino]benzamide

1.2 Other means of identification

Product number -
Other names Benzamide,N-(6-amino-1,2,3,4-tetrahydro-2,4-dioxo-1,3-dipropyl-5-pyrimidinyl)-3,5-dichloro-2-[(trifluoroacetyl)amino]-(9CI)

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:154623-75-3 SDS

154623-75-3Relevant academic research and scientific papers

Synthesis and A1-adenosine receptors affinities of purino[7,8- c]quinazoline-8,10(9H,11H)-diones as rigid analogues of 8-arylxanthines

Ceccarelli,D'Alessandro,Magnante,Scuri,Zanarella

, p. 1301 - 1312 (2007/10/02)

Title compounds were prepared by a cyclocondensation reaction between 8- (2-aminophenyl)xanthines and trialkyl orthoesters. Some of them showed activities as A1-adenosine receptor antagonists with binding values in the micromolar range. Results

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