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55854-97-2

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55854-97-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55854-97-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,8,5 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 55854-97:
(7*5)+(6*5)+(5*8)+(4*5)+(3*4)+(2*9)+(1*7)=162
162 % 10 = 2
So 55854-97-2 is a valid CAS Registry Number.

55854-97-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4,6,7,12,12b-hexahydro-1H-indolo[2,3-a]quinolizin-2-one

1.2 Other means of identification

Product number -
Other names 1,2,3,4,6,7,12,12b-octahydroindolo<quinolizin-2-one

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:55854-97-2 SDS

55854-97-2Downstream Products

55854-97-2Relevant articles and documents

Quinolizidine compound and the manufacturing method thereof

-

Paragraph 0324-0330; 0498-0504, (2021/02/19)

Provided are benzoquinolizidine and indoloquinolizidine derivative compounds prepared by performing Mannich reaction using Azza-Michahael response and DDQ oxidizer from tetrahydroisoquinoline or tryptoline, and to a process for preparing the same. The met

Access to electron-rich arene-fused hexahydroquinolizinones through a gold-catalysis-initiated cascade process

Liu, Lianzhu,Zhang, Liming

, p. 7301 - 7304 (2012/09/08)

Golden Cascade: With a tethered, electron-rich arene as the internal nucleophile, a gold-catalyzed amide cyclization to an alkyne initiates a cascade process that ends with a Ferrier rearrangement. Electron-rich arene-bearing hexahydroquinolizin-2-ones are formed in good yields and can be converted into indole alkaloids in only a few steps. Copyright

Synthesis of indolo[2,3-a]quinolizidin-2-one

Giri,Sankar

, p. 3095 - 3100 (2007/10/02)

Ketalization of 3-acetyl-1,2,6,7,12,12b-hexahydroindolo[2,3-a]quinolizin-2-one (2) with ethylene glycol followed by sodium borohydride reduction and acid hydrolysis gave indolo[2,3-a]quinolizidin-2-one (1) in very high overall yield.

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