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9-Acridinamine, 1,2,3,4,5,6,7,8-octahydro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13415-07-1

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13415-07-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13415-07-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,4,1 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13415-07:
(7*1)+(6*3)+(5*4)+(4*1)+(3*5)+(2*0)+(1*7)=71
71 % 10 = 1
So 13415-07-1 is a valid CAS Registry Number.

13415-07-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,4,5,6,7,8-octahydroacridin-9-amine

1.2 Other means of identification

Product number -
Other names 9-amino-1,2,3,4,5,6,7,8-octahydroacridine

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:13415-07-1 SDS

13415-07-1Relevant academic research and scientific papers

Convenient preparation of tacrine derivatives by the reduction of 9-aminoacridines with nickel-aluminum alloy

Kamata, Kichinosuke,Tominaga, Yoh-Ichi,Tori-I, Akiyoshi,Thiemann, Thies,Takahashi, Kazufumi,Mataka, Shuntaro

, p. 1683 - 1688 (2007/10/03)

9-Amino-1,2,3,4-tetrahydro- and 9-amino-1,2,3,4,5,6,7,8-octahydro-acridine derivatives (2 and 3) were conveniently prepared in the reduction of the corresponding 2-substituted 9-aminoacridines (1a-f) with nickel-aluminum alloy under basic conditions. The reduction is dependent upon the nature of the substituent in the 2-position of the starting 9-aminoacridines.

Selective Hydrogenation of 9-Aminoacridine over Supported Noble Metal Catalysts

Sakanishi, Kinya,Mochida, Isao,Okazaki, Hiroshi,Soeda, Mahito

, p. 319 - 322 (2007/10/02)

The selective hydrogenation of 9-aminoacridine (1) into 1,2,3,4-tetrahydro-derivative (2) was searched using noble metal catalysts (Pd, Rh, Pt, and Ru) at around 80 deg C and 60 atm of H2.The Pd/Al2O3 catalyst was found most selective to produce 2 in a higher yield of 60 percent at a conversion of 97 percent.The hydrogenation pathway of 1 is discussed in comparison with that of acridine.

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