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7H-Cyclopenta[h]quinolin-5-amine, 8,9-dihydro-6-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

75265-95-1

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75265-95-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75265-95-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,2,6 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 75265-95:
(7*7)+(6*5)+(5*2)+(4*6)+(3*5)+(2*9)+(1*5)=151
151 % 10 = 1
So 75265-95-1 is a valid CAS Registry Number.

75265-95-1SDS

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-phenyl-8,9-dihydro-7H-cyclopenta[h]quinolin-5-amine

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:75265-95-1 SDS

75265-95-1Downstream Products

75265-95-1Relevant academic research and scientific papers

METABOLIC FORMATION AND CHEMICAL SYNTHESIS OF 5,6-CYCLOPENTENO-4,11-DIHYDRO-3H-PYRIDOCARBAZOL-3-ONE, THE MAJOR INTESTINAL BACTERIAL METABOLITE OF THE PYROLYSIS MUTAGEN 5,6-CYCLOPENTENO-11H-PYRIDOCARBAZOLE (LYS-P-1)

Kingston, David G. I.,Shu, Yue-Zhong,Tassel, Roger L. Van,Wilkins, Tracy D.

, p. 1821 - 1830 (2007/10/02)

Anaerobic incubation of the lysine pyrolysis mutagen 5,6-cyclopenteno-11H-pyridocarbazole (Lys-P-1,3) with human intestinal bacterial mixtures yielded the major metabolite 5,6-cyclopenteno-4,11-dihydro-3H-pyridocarbazol-3-one (3-OH-Lys-P-1,4).The metabolite (4) has been synthesized from 4-aminoindane in six steps.NAD and NADP significantly enhanced the metabolism, suggesting that the transformation of 3 leading to 4 involves a hydration and subsequent dehydrogenation processes.

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